Canonical Allele Identifier: CA1949587868

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253227C= , CM000673.2:g.5253227C=	GRCh38
NC_000011.9:g.5274457C= , CM000673.1:g.5274457C=	GRCh37
NC_000011.8:g.5231033C=	NCBI36
NG_000007.3:g.44389G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.*50G= MANE Select	ENSP00000338082.4:n.*50G=
ENST00000380252.6:c.*50G=	ENSP00000369602.2:n.*50G=
ENST00000642908.1:c.315+1065G=	ENSP00000495346.1:n.315+1065G=
ENST00000647543.1:c.378+116G=	ENSP00000496470.1:n.378+116G=
ENST00000336906.4:c.*50G=	ENSP00000338082.4:n.*50G=
ENST00000380252.5:c.*50G=	ENSP00000369602.1:n.*50G=
ENST00000380259.6:c.*50G=	ENSP00000369609.2:n.*50G=
ENST00000620888.4:c.315+1065G=	ENSP00000479637.1:n.315+1065G=
NM_000184.2:c.*50G=	NP_000175.1:n.*50G=
NM_000184.3:c.*50G= MANE Select	NP_000175.1:n.*50G=