Canonical Allele Identifier: CA1949577455

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254419G= , CM000673.2:g.5254419G=	GRCh38
NC_000011.9:g.5275649G= , CM000673.1:g.5275649G=	GRCh37
NC_000011.8:g.5232225G=	NCBI36
NG_000007.3:g.43197C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.188C= MANE Select	ENSP00000338082.4:p.Ala63=
ENST00000380252.6:c.23C=	ENSP00000369602.2:p.Ala8=
ENST00000380259.7:c.1734C=	ENSP00000369609.3:n.1734C=
ENST00000642908.1:c.188C=	ENSP00000495346.1:p.Ala63=
ENST00000647543.1:c.188C=	ENSP00000496470.1:p.Ala63=
ENST00000336906.4:c.188C=	ENSP00000338082.4:p.Ala63=
ENST00000380252.5:c.158C=	ENSP00000369602.1:p.Ala53=
ENST00000380259.6:c.188C=	ENSP00000369609.2:p.Ala63=
ENST00000444587.1:c.*57C=	ENSP00000488218.1:n.*57C=
ENST00000620888.4:c.188C=	ENSP00000479637.1:p.Ala63=
ENST00000624109.1:c.167G=	ENSP00000485458.1:p.Cys56=
NM_000184.2:c.188C=	NP_000175.1:p.Ala63=
NM_000184.3:c.188C= MANE Select	NP_000175.1:p.Ala63=