Canonical Allele Identifier: CA1949577765

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254698T= , CM000673.2:g.5254698T=	GRCh38
NC_000011.9:g.5275928T= , CM000673.1:g.5275928T=	GRCh37
NC_000011.8:g.5232504T=	NCBI36
NG_000007.3:g.42918A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.31A= MANE Select	ENSP00000338082.4:p.Thr11=
ENST00000380252.6:c.-73-184A=	ENSP00000369602.2:n.-73-184A=
ENST00000380259.7:c.1577A=	ENSP00000369609.3:n.1577A=
ENST00000642908.1:c.31A=	ENSP00000495346.1:p.Thr11=
ENST00000647543.1:c.31A=	ENSP00000496470.1:p.Thr11=
ENST00000336906.4:c.31A=	ENSP00000338082.4:p.Thr11=
ENST00000380252.5:c.63-184A=	ENSP00000369602.1:n.63-184A=
ENST00000380259.6:c.31A=	ENSP00000369609.2:p.Thr11=
ENST00000444587.1:c.31A=	ENSP00000488218.1:p.Thr11=
ENST00000620888.4:c.31A=	ENSP00000479637.1:p.Thr11=
ENST00000624109.1:c.327T=	ENSP00000485458.1:p.Ser109=
NM_000184.2:c.31A=	NP_000175.1:p.Thr11=
NM_000184.3:c.31A= MANE Select	NP_000175.1:p.Thr11=