Canonical Allele Identifier: CA1949576977

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254097T= , CM000673.2:g.5254097T=	GRCh38
NC_000011.9:g.5275327T= , CM000673.1:g.5275327T=	GRCh37
NC_000011.8:g.5231903T=	NCBI36
NG_000007.3:g.43519A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.315+195A= MANE Select	ENSP00000338082.4:n.315+195A=
ENST00000380252.6:c.150+195A=	ENSP00000369602.2:n.150+195A=
ENST00000642908.1:c.315+195A=	ENSP00000495346.1:n.315+195A=
ENST00000647543.1:c.315+195A=	ENSP00000496470.1:n.315+195A=
ENST00000336906.4:c.315+195A=	ENSP00000338082.4:n.315+195A=
ENST00000380252.5:c.285+195A=	ENSP00000369602.1:n.285+195A=
ENST00000380259.6:c.315+195A=	ENSP00000369609.2:n.315+195A=
ENST00000444587.1:c.*184+195A=	ENSP00000488218.1:n.*184+195A=
ENST00000620888.4:c.315+195A=	ENSP00000479637.1:n.315+195A=
ENST00000624109.1:c.43-198T=	ENSP00000485458.1:n.43-198T=
NM_000184.2:c.315+195A=	NP_000175.1:n.315+195A=
NM_000184.3:c.315+195A= MANE Select	NP_000175.1:n.315+195A=