Canonical Allele Identifier: CA1949577458

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254422T= , CM000673.2:g.5254422T=	GRCh38
NC_000011.9:g.5275652T= , CM000673.1:g.5275652T=	GRCh37
NC_000011.8:g.5232228T=	NCBI36
NG_000007.3:g.43194A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336906.6:c.185A= MANE Select	ENSP00000338082.4:p.Lys62=
ENST00000380252.6:c.20A=	ENSP00000369602.2:p.Lys7=
ENST00000380259.7:c.1731A=	ENSP00000369609.3:n.1731A=
ENST00000642908.1:c.185A=	ENSP00000495346.1:p.Lys62=
ENST00000647543.1:c.185A=	ENSP00000496470.1:p.Lys62=
ENST00000336906.4:c.185A=	ENSP00000338082.4:p.Lys62=
ENST00000380252.5:c.155A=	ENSP00000369602.1:p.Lys52=
ENST00000380259.6:c.185A=	ENSP00000369609.2:p.Lys62=
ENST00000444587.1:c.*54A=	ENSP00000488218.1:n.*54A=
ENST00000620888.4:c.185A=	ENSP00000479637.1:p.Lys62=
ENST00000624109.1:c.170T=	ENSP00000485458.1:p.Leu57=
NM_000184.2:c.185A=	NP_000175.1:p.Lys62=
NM_000184.3:c.185A= MANE Select	NP_000175.1:p.Lys62=