Canonical Allele Identifier: CA1949587848

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253207A= , CM000673.2:g.5253207A=	GRCh38
NC_000011.9:g.5274437A= , CM000673.1:g.5274437A=	GRCh37
NC_000011.8:g.5231013A=	NCBI36
NG_000007.3:g.44409T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.*70T= MANE Select	ENSP00000338082.4:n.*70T=
ENST00000380252.6:c.*70T=	ENSP00000369602.2:n.*70T=
ENST00000642908.1:c.315+1085T=	ENSP00000495346.1:n.315+1085T=
ENST00000647543.1:c.378+136T=	ENSP00000496470.1:n.378+136T=
ENST00000336906.4:c.*70T=	ENSP00000338082.4:n.*70T=
ENST00000380252.5:c.*70T=	ENSP00000369602.1:n.*70T=
ENST00000380259.6:c.*70T=	ENSP00000369609.2:n.*70T=
ENST00000620888.4:c.315+1085T=	ENSP00000479637.1:n.315+1085T=
NM_000184.2:c.*70T=	NP_000175.1:n.*70T=
NM_000184.3:c.*70T= MANE Select	NP_000175.1:n.*70T=