Canonical Allele Identifier: CA2200883287
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177362A= , CM000678.2:g.177362A= GRCh38
NC_000016.9:g.227361A= , CM000678.1:g.227361A= GRCh37
NC_000016.8:g.167361A= NCBI36
NG_000006.1:g.38225A=
NG_059186.1:g.5712A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.380A= MANE Select ENSP00000322421.5:p.Asp127=
ENST00000397797.1:c.284A= ENSP00000380899.1:p.Asp95=
ENST00000472694.1:n.516A=
NM_000558.4:c.380A= NP_000549.1:p.Asp127=
NM_000558.5:c.380A= MANE Select NP_000549.1:p.Asp127=