Canonical Allele Identifier: CA1949575535

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253368T= , CM000673.2:g.5253368T=	GRCh38
NC_000011.9:g.5274598T= , CM000673.1:g.5274598T=	GRCh37
NC_000011.8:g.5231174T=	NCBI36
NG_000007.3:g.44248A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000184.3:c.353A= MANE Select	NP_000175.1:p.His118=
ENST00000336906.6:c.353A= MANE Select	ENSP00000338082.4:p.His118=
NM_000184.2:c.353A=	NP_000175.1:p.His118=
ENST00000336906.4:c.353A=	ENSP00000338082.4:p.His118=
ENST00000380252.5:c.323A=	ENSP00000369602.1:p.His108=
ENST00000380252.6:c.188A=	ENSP00000369602.2:p.His63=
ENST00000380259.6:c.353A=	ENSP00000369609.2:p.His118=
ENST00000620888.4:c.315+924A=	ENSP00000479637.1:n.315+924A=
ENST00000624109.1:c.2T=	ENSP00000485458.1:p.Met1=
ENST00000642908.1:c.315+924A=	ENSP00000495346.1:n.315+924A=
ENST00000647543.1:c.353A=	ENSP00000496470.1:p.His118=