Canonical Allele Identifier: CA393995844
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177314C>G , CM000678.2:g.177314C>G GRCh38
NC_000016.9:g.227313C>G , CM000678.1:g.227313C>G GRCh37
NC_000016.8:g.167313C>G NCBI36
NG_000006.1:g.38177C>G
NG_059186.1:g.5664C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.332C>G MANE Select ENSP00000322421.5:p.Ala111Gly
ENST00000397797.1:c.236C>G ENSP00000380899.1:p.Ala79Gly
ENST00000472694.1:n.468C>G
NM_000558.4:c.332C>G NP_000549.1:p.Ala111Gly
NM_000558.5:c.332C>G MANE Select NP_000549.1:p.Ala111Gly