Canonical Allele Identifier: CA2200883099

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177099C= , CM000678.2:g.177099C=	GRCh38
NC_000016.9:g.227098C= , CM000678.1:g.227098C=	GRCh37
NC_000016.8:g.167098C=	NCBI36
NG_000006.1:g.37962C=
NG_059186.1:g.5449C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.266C= MANE Select	ENSP00000322421.5:p.Ala89=
ENST00000397797.1:c.170C=	ENSP00000380899.1:p.Ala57=
ENST00000472694.1:n.402C=
ENST00000487791.1:n.235C=
NM_000558.4:c.266C=	NP_000549.1:p.Ala89=
NM_000558.5:c.266C= MANE Select	NP_000549.1:p.Ala89=