Canonical Allele Identifier: CA1949577402

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254398G= , CM000673.2:g.5254398G=	GRCh38
NC_000011.9:g.5275628G= , CM000673.1:g.5275628G=	GRCh37
NC_000011.8:g.5232204G=	NCBI36
NG_000007.3:g.43218C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.209C= MANE Select	ENSP00000338082.4:p.Thr70=
ENST00000380252.6:c.44C=	ENSP00000369602.2:p.Thr15=
ENST00000380259.7:c.1755C=	ENSP00000369609.3:n.1755C=
ENST00000642908.1:c.209C=	ENSP00000495346.1:p.Thr70=
ENST00000647543.1:c.209C=	ENSP00000496470.1:p.Thr70=
ENST00000336906.4:c.209C=	ENSP00000338082.4:p.Thr70=
ENST00000380252.5:c.179C=	ENSP00000369602.1:p.Thr60=
ENST00000380259.6:c.209C=	ENSP00000369609.2:p.Thr70=
ENST00000444587.1:c.*78C=	ENSP00000488218.1:n.*78C=
ENST00000620888.4:c.209C=	ENSP00000479637.1:p.Thr70=
ENST00000624109.1:c.146G=	ENSP00000485458.1:p.Ser49=
NM_000184.2:c.209C=	NP_000175.1:p.Thr70=
NM_000184.3:c.209C= MANE Select	NP_000175.1:p.Thr70=