Canonical Allele Identifier: CA1949575393

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253315T= , CM000673.2:g.5253315T=	GRCh38
NC_000011.9:g.5274545T= , CM000673.1:g.5274545T=	GRCh37
NC_000011.8:g.5231121T=	NCBI36
NG_000007.3:g.44301A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.406A= MANE Select	ENSP00000338082.4:p.Thr136=
ENST00000380252.6:c.241A=	ENSP00000369602.2:p.Thr81=
ENST00000642908.1:c.315+977A=	ENSP00000495346.1:n.315+977A=
ENST00000647543.1:c.378+28A=	ENSP00000496470.1:n.378+28A=
ENST00000336906.4:c.406A=	ENSP00000338082.4:p.Thr136=
ENST00000380252.5:c.376A=	ENSP00000369602.1:p.Thr126=
ENST00000380259.6:c.406A=	ENSP00000369609.2:p.Thr136=
ENST00000620888.4:c.315+977A=	ENSP00000479637.1:n.315+977A=
NM_000184.2:c.406A=	NP_000175.1:p.Thr136=
NM_000184.3:c.406A= MANE Select	NP_000175.1:p.Thr136=