Canonical Allele Identifier: CA1949577271

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254324C= , CM000673.2:g.5254324C=	GRCh38
NC_000011.9:g.5275554C= , CM000673.1:g.5275554C=	GRCh37
NC_000011.8:g.5232130C=	NCBI36
NG_000007.3:g.43292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.283G= MANE Select	ENSP00000338082.4:p.Asp95=
ENST00000380252.6:c.118G=	ENSP00000369602.2:p.Asp40=
ENST00000642908.1:c.283G=	ENSP00000495346.1:p.Asp95=
ENST00000647543.1:c.283G=	ENSP00000496470.1:p.Asp95=
ENST00000336906.4:c.283G=	ENSP00000338082.4:p.Asp95=
ENST00000380252.5:c.253G=	ENSP00000369602.1:p.Asp85=
ENST00000380259.6:c.283G=	ENSP00000369609.2:p.Asp95=
ENST00000444587.1:c.*152G=	ENSP00000488218.1:n.*152G=
ENST00000620888.4:c.283G=	ENSP00000479637.1:p.Asp95=
ENST00000624109.1:c.72C=	ENSP00000485458.1:p.Val24=
NM_000184.2:c.283G=	NP_000175.1:p.Asp95=
NM_000184.3:c.283G= MANE Select	NP_000175.1:p.Asp95=