Canonical Allele Identifier: CA2200883034

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177011G= , CM000678.2:g.177011G=	GRCh38
NC_000016.9:g.227010G= , CM000678.1:g.227010G=	GRCh37
NC_000016.8:g.167010G=	NCBI36
NG_000006.1:g.37874G=
NG_059186.1:g.5361G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320868.9:c.178G= MANE Select	ENSP00000322421.5:p.Gly60=
ENST00000397797.1:c.82G=	ENSP00000380899.1:p.Gly28=
ENST00000472694.1:n.314G=
ENST00000487791.1:n.147G=
NM_000558.4:c.178G=	NP_000549.1:p.Gly60=
NM_000558.5:c.178G= MANE Select	NP_000549.1:p.Gly60=