Canonical Allele Identifier: CA1949575454

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253344T= , CM000673.2:g.5253344T=	GRCh38
NC_000011.9:g.5274574T= , CM000673.1:g.5274574T=	GRCh37
NC_000011.8:g.5231150T=	NCBI36
NG_000007.3:g.44272A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000184.3:c.377A= MANE Select	NP_000175.1:p.Glu126=
ENST00000336906.6:c.377A= MANE Select	ENSP00000338082.4:p.Glu126=
NM_000184.2:c.377A=	NP_000175.1:p.Glu126=
ENST00000336906.4:c.377A=	ENSP00000338082.4:p.Glu126=
ENST00000380252.5:c.347A=	ENSP00000369602.1:p.Glu116=
ENST00000380252.6:c.212A=	ENSP00000369602.2:p.Glu71=
ENST00000380259.6:c.377A=	ENSP00000369609.2:p.Glu126=
ENST00000620888.4:c.315+948A=	ENSP00000479637.1:n.315+948A=
ENST00000642908.1:c.315+948A=	ENSP00000495346.1:n.315+948A=
ENST00000647543.1:c.377A=	ENSP00000496470.1:p.Glu126=