Seven ClinVar variants in the HBB gene

Choose a variant with a button, or click it in the picture. The picture, the message below the buttons and the table give the same information.

HBB on GRCh38, chr11:5,225,464-5,227,071. The gene is read from right to left (reverse strand). Tall boxes are coding sequence. pathogenic or likely pathogenic benign

Variants, in order along the chromosome

The same variants as a table (ClinVar release of 4 October 2026)

Variant	GRCh38 position and change	In HBB	Protein	Known as	ClinVar