Canonical Allele Identifier: CA393993542
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1444027231
gnomAD v4: 16-173224-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173224C>A , CM000678.2:g.173224C>A GRCh38
NC_000016.9:g.223223C>A , CM000678.1:g.223223C>A GRCh37
NC_000016.8:g.163223C>A NCBI36
NG_000006.1:g.34087C>A
NG_059186.1:g.1574C>A
NG_059271.1:g.5378C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.195C>A MANE Select ENSP00000251595.6:p.Asp65Glu
ENST00000251595.10:c.195C>A ENSP00000251595.6:p.Asp65Glu
ENST00000397806.1:c.99C>A ENSP00000380908.1:p.Asp33Glu
ENST00000482565.1:n.331C>A
ENST00000484216.1:n.164C>A
NM_000517.4:c.195C>A NP_000508.1:p.Asp65Glu
NM_000517.6:c.195C>A MANE Select NP_000508.1:p.Asp65Glu