Canonical Allele Identifier: CA2200883019

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.176988G= , CM000678.2:g.176988G=	GRCh38
NC_000016.9:g.226987G= , CM000678.1:g.226987G=	GRCh37
NC_000016.8:g.166987G=	NCBI36
NG_000006.1:g.37851G=
NG_059186.1:g.5338G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.155G= MANE Select	ENSP00000322421.5:p.Gly52=
ENST00000397797.1:c.59G=	ENSP00000380899.1:p.Gly20=
ENST00000472694.1:n.291G=
ENST00000487791.1:n.124G=
NM_000558.4:c.155G=	NP_000549.1:p.Gly52=
NM_000558.5:c.155G= MANE Select	NP_000549.1:p.Gly52=