Canonical Allele Identifier: CA393995145
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176993G>A , CM000678.2:g.176993G>A GRCh38
NC_000016.9:g.226992G>A , CM000678.1:g.226992G>A GRCh37
NC_000016.8:g.166992G>A NCBI36
NG_000006.1:g.37856G>A
NG_059186.1:g.5343G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.160G>A MANE Select ENSP00000322421.5:p.Ala54Thr
ENST00000397797.1:c.64G>A ENSP00000380899.1:p.Ala22Thr
ENST00000472694.1:n.296G>A
ENST00000487791.1:n.129G>A
NM_000558.4:c.160G>A NP_000549.1:p.Ala54Thr
NM_000558.5:c.160G>A MANE Select NP_000549.1:p.Ala54Thr