Canonical Allele Identifier: CA1949577529

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254503A= , CM000673.2:g.5254503A=	GRCh38
NC_000011.9:g.5275733A= , CM000673.1:g.5275733A=	GRCh37
NC_000011.8:g.5232309A=	NCBI36
NG_000007.3:g.43113T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.104T= MANE Select	ENSP00000338082.4:p.Val35=
ENST00000380252.6:c.-62T=	ENSP00000369602.2:n.-62T=
ENST00000380259.7:c.1650T=	ENSP00000369609.3:n.1650T=
ENST00000642908.1:c.104T=	ENSP00000495346.1:p.Val35=
ENST00000647543.1:c.104T=	ENSP00000496470.1:p.Val35=
ENST00000336906.4:c.104T=	ENSP00000338082.4:p.Val35=
ENST00000380252.5:c.74T=	ENSP00000369602.1:p.Val25=
ENST00000380259.6:c.104T=	ENSP00000369609.2:p.Val35=
ENST00000444587.1:c.66T=	ENSP00000488218.1:p.Cys22=
ENST00000620888.4:c.104T=	ENSP00000479637.1:p.Val35=
ENST00000624109.1:c.251A=	ENSP00000485458.1:p.Asp84=
NM_000184.2:c.104T=	NP_000175.1:p.Val35=
NM_000184.3:c.104T= MANE Select	NP_000175.1:p.Val35=