Canonical Allele Identifier: CA393994944
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176753G>A , CM000678.2:g.176753G>A GRCh38
NC_000016.9:g.226752G>A , CM000678.1:g.226752G>A GRCh37
NC_000016.8:g.166752G>A NCBI36
NG_000006.1:g.37616G>A
NG_059186.1:g.5103G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.37G>A MANE Select ENSP00000322421.5:p.Ala13Thr
ENST00000397797.1:c.-11G>A ENSP00000380899.1:n.-11G>A
ENST00000472694.1:n.56G>A
ENST00000487791.1:n.6G>A
NM_000558.4:c.37G>A NP_000549.1:p.Ala13Thr
NM_000558.5:c.37G>A MANE Select NP_000549.1:p.Ala13Thr