Canonical Allele Identifier: CA1949577847

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254757C= , CM000673.2:g.5254757C=	GRCh38
NC_000011.9:g.5275987C= , CM000673.1:g.5275987C=	GRCh37
NC_000011.8:g.5232563C=	NCBI36
NG_000007.3:g.42859G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.-29G= MANE Select	ENSP00000338082.4:n.-29G=
ENST00000380252.6:c.-73-243G=	ENSP00000369602.2:n.-73-243G=
ENST00000380259.7:c.1518G=	ENSP00000369609.3:n.1518G=
ENST00000642908.1:c.-29G=	ENSP00000495346.1:n.-29G=
ENST00000647543.1:c.-29G=	ENSP00000496470.1:n.-29G=
ENST00000336906.4:c.-29G=	ENSP00000338082.4:n.-29G=
ENST00000380252.5:c.63-243G=	ENSP00000369602.1:n.63-243G=
ENST00000380259.6:c.-29G=	ENSP00000369609.2:n.-29G=
ENST00000620888.4:c.-29G=	ENSP00000479637.1:n.-29G=
ENST00000624109.1:c.386C=	ENSP00000485458.1:p.Thr129=
NM_000184.2:c.-29G=	NP_000175.1:n.-29G=
NM_000184.3:c.-29G= MANE Select	NP_000175.1:n.-29G=