Canonical Allele Identifier: CA2200883357
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177450C= , CM000678.2:g.177450C= GRCh38
NC_000016.9:g.227449C= , CM000678.1:g.227449C= GRCh37
NC_000016.8:g.167449C= NCBI36
NG_000006.1:g.38313C=
NG_059186.1:g.5800C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.*39C= MANE Select ENSP00000322421.5:n.*39C=
ENST00000397797.1:c.*39C= ENSP00000380899.1:n.*39C=
ENST00000472694.1:n.604C=
NM_000558.4:c.*39C= NP_000549.1:n.*39C=
NM_000558.5:c.*39C= MANE Select NP_000549.1:n.*39C=