Canonical Allele Identifier: CA393995151
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176994C>G , CM000678.2:g.176994C>G GRCh38
NC_000016.9:g.226993C>G , CM000678.1:g.226993C>G GRCh37
NC_000016.8:g.166993C>G NCBI36
NG_000006.1:g.37857C>G
NG_059186.1:g.5344C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.161C>G MANE Select ENSP00000322421.5:p.Ala54Gly
ENST00000397797.1:c.65C>G ENSP00000380899.1:p.Ala22Gly
ENST00000472694.1:n.297C>G
ENST00000487791.1:n.130C>G
NM_000558.4:c.161C>G NP_000549.1:p.Ala54Gly
NM_000558.5:c.161C>G MANE Select NP_000549.1:p.Ala54Gly