Canonical Allele Identifier: CA2200882772
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176682T= , CM000678.2:g.176682T= GRCh38
NC_000016.9:g.226681T= , CM000678.1:g.226681T= GRCh37
NC_000016.8:g.166681T= NCBI36
NG_000006.1:g.37545T=
NG_059186.1:g.5032T=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-35T= MANE Select ENSP00000322421.5:n.-35T=
NM_000558.4:c.-35T= NP_000549.1:n.-35T=
NM_000558.5:c.-35T= MANE Select NP_000549.1:n.-35T=