Canonical Allele Identifier: CA1949577522

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254488T= , CM000673.2:g.5254488T=	GRCh38
NC_000011.9:g.5275718T= , CM000673.1:g.5275718T=	GRCh37
NC_000011.8:g.5232294T=	NCBI36
NG_000007.3:g.43128A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.119A= MANE Select	ENSP00000338082.4:p.Gln40=
ENST00000380252.6:c.-47A=	ENSP00000369602.2:n.-47A=
ENST00000380259.7:c.1665A=	ENSP00000369609.3:n.1665A=
ENST00000642908.1:c.119A=	ENSP00000495346.1:p.Gln40=
ENST00000647543.1:c.119A=	ENSP00000496470.1:p.Gln40=
ENST00000336906.4:c.119A=	ENSP00000338082.4:p.Gln40=
ENST00000380252.5:c.89A=	ENSP00000369602.1:p.Gln30=
ENST00000380259.6:c.119A=	ENSP00000369609.2:p.Gln40=
ENST00000444587.1:c.81A=	ENSP00000488218.1:p.Pro27=
ENST00000620888.4:c.119A=	ENSP00000479637.1:p.Gln40=
ENST00000624109.1:c.236T=	ENSP00000485458.1:p.Leu79=
NM_000184.2:c.119A=	NP_000175.1:p.Gln40=
NM_000184.3:c.119A= MANE Select	NP_000175.1:p.Gln40=