Canonical Allele Identifier: CA1949577510

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254475G= , CM000673.2:g.5254475G=	GRCh38
NC_000011.9:g.5275705G= , CM000673.1:g.5275705G=	GRCh37
NC_000011.8:g.5232281G=	NCBI36
NG_000007.3:g.43141C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.132C= MANE Select	ENSP00000338082.4:p.Asp44=
ENST00000380252.6:c.-34C=	ENSP00000369602.2:n.-34C=
ENST00000380259.7:c.1678C=	ENSP00000369609.3:n.1678C=
ENST00000642908.1:c.132C=	ENSP00000495346.1:p.Asp44=
ENST00000647543.1:c.132C=	ENSP00000496470.1:p.Asp44=
ENST00000336906.4:c.132C=	ENSP00000338082.4:p.Asp44=
ENST00000380252.5:c.102C=	ENSP00000369602.1:p.Asp34=
ENST00000380259.6:c.132C=	ENSP00000369609.2:p.Asp44=
ENST00000444587.1:c.*1C=	ENSP00000488218.1:n.*1C=
ENST00000620888.4:c.132C=	ENSP00000479637.1:p.Asp44=
ENST00000624109.1:c.223G=	ENSP00000485458.1:p.Val75=
NM_000184.2:c.132C=	NP_000175.1:p.Asp44=
NM_000184.3:c.132C= MANE Select	NP_000175.1:p.Asp44=