Canonical Allele Identifier: CA1949577792

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254712T= , CM000673.2:g.5254712T=	GRCh38
NC_000011.9:g.5275942T= , CM000673.1:g.5275942T=	GRCh37
NC_000011.8:g.5232518T=	NCBI36
NG_000007.3:g.42904A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000184.3:c.17A= MANE Select	NP_000175.1:p.Glu6=
ENST00000336906.6:c.17A= MANE Select	ENSP00000338082.4:p.Glu6=
NM_000184.2:c.17A=	NP_000175.1:p.Glu6=
ENST00000336906.4:c.17A=	ENSP00000338082.4:p.Glu6=
ENST00000380252.5:c.63-198A=	ENSP00000369602.1:n.63-198A=
ENST00000380252.6:c.-73-198A=	ENSP00000369602.2:n.-73-198A=
ENST00000380259.6:c.17A=	ENSP00000369609.2:p.Glu6=
ENST00000380259.7:c.1563A=	ENSP00000369609.3:n.1563A=
ENST00000444587.1:c.17A=	ENSP00000488218.1:p.Glu6=
ENST00000620888.4:c.17A=	ENSP00000479637.1:p.Glu6=
ENST00000624109.1:c.341T=	ENSP00000485458.1:p.Leu114=
ENST00000642908.1:c.17A=	ENSP00000495346.1:p.Glu6=
ENST00000647543.1:c.17A=	ENSP00000496470.1:p.Glu6=