Canonical Allele Identifier: CA2200883271

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177334T= , CM000678.2:g.177334T=	GRCh38
NC_000016.9:g.227333T= , CM000678.1:g.227333T=	GRCh37
NC_000016.8:g.167333T=	NCBI36
NG_000006.1:g.38197T=
NG_059186.1:g.5684T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320868.9:c.352T= MANE Select	ENSP00000322421.5:p.Phe118=
ENST00000397797.1:c.256T=	ENSP00000380899.1:p.Phe86=
ENST00000472694.1:n.488T=
NM_000558.4:c.352T=	NP_000549.1:p.Phe118=
NM_000558.5:c.352T= MANE Select	NP_000549.1:p.Phe118=