Canonical Allele Identifier: CA1949577281

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254330G= , CM000673.2:g.5254330G=	GRCh38
NC_000011.9:g.5275560G= , CM000673.1:g.5275560G=	GRCh37
NC_000011.8:g.5232136G=	NCBI36
NG_000007.3:g.43286C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000184.3:c.277C= MANE Select	NP_000175.1:p.His93=
ENST00000336906.6:c.277C= MANE Select	ENSP00000338082.4:p.His93=
NM_000184.2:c.277C=	NP_000175.1:p.His93=
ENST00000336906.4:c.277C=	ENSP00000338082.4:p.His93=
ENST00000380252.5:c.247C=	ENSP00000369602.1:p.His83=
ENST00000380252.6:c.112C=	ENSP00000369602.2:p.His38=
ENST00000380259.6:c.277C=	ENSP00000369609.2:p.His93=
ENST00000444587.1:c.*146C=	ENSP00000488218.1:n.*146C=
ENST00000620888.4:c.277C=	ENSP00000479637.1:p.His93=
ENST00000624109.1:c.78G=	ENSP00000485458.1:p.Val26=
ENST00000642908.1:c.277C=	ENSP00000495346.1:p.His93=
ENST00000647543.1:c.277C=	ENSP00000496470.1:p.His93=