Canonical Allele Identifier: CA1949577225

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254303C= , CM000673.2:g.5254303C=	GRCh38
NC_000011.9:g.5275533C= , CM000673.1:g.5275533C=	GRCh37
NC_000011.8:g.5232109C=	NCBI36
NG_000007.3:g.43313G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000184.3:c.304G= MANE Select	NP_000175.1:p.Glu102=
ENST00000336906.6:c.304G= MANE Select	ENSP00000338082.4:p.Glu102=
NM_000184.2:c.304G=	NP_000175.1:p.Glu102=
ENST00000336906.4:c.304G=	ENSP00000338082.4:p.Glu102=
ENST00000380252.5:c.274G=	ENSP00000369602.1:p.Glu92=
ENST00000380252.6:c.139G=	ENSP00000369602.2:p.Glu47=
ENST00000380259.6:c.304G=	ENSP00000369609.2:p.Glu102=
ENST00000444587.1:c.*173G=	ENSP00000488218.1:n.*173G=
ENST00000620888.4:c.304G=	ENSP00000479637.1:p.Glu102=
ENST00000624109.1:c.51C=	ENSP00000485458.1:p.Leu17=
ENST00000642908.1:c.304G=	ENSP00000495346.1:p.Glu102=
ENST00000647543.1:c.304G=	ENSP00000496470.1:p.Glu102=