Canonical Allele Identifier: CA1949577111

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254232_5254233delinsCA , CM000673.2:g.5254232_5254233delinsCA	GRCh38
NC_000011.9:g.5275462_5275463delinsCA , CM000673.1:g.5275462_5275463delinsCA	GRCh37
NC_000011.8:g.5232038_5232039delinsCA	NCBI36
NG_000007.3:g.43383_43384delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.315+59_315+60delinsTG MANE Select	ENSP00000338082.4:n.315+59_315+60delinsTG
ENST00000380252.6:c.150+59_150+60delinsTG	ENSP00000369602.2:n.150+59_150+60delinsTG
ENST00000642908.1:c.315+59_315+60delinsTG	ENSP00000495346.1:n.315+59_315+60delinsTG
ENST00000647543.1:c.315+59_315+60delinsTG	ENSP00000496470.1:n.315+59_315+60delinsTG
ENST00000336906.4:c.315+59_315+60delinsTG	ENSP00000338082.4:n.315+59_315+60delinsTG
ENST00000380252.5:c.285+59_285+60delinsTG	ENSP00000369602.1:n.285+59_285+60delinsTG
ENST00000380259.6:c.315+59_315+60delinsTG	ENSP00000369609.2:n.315+59_315+60delinsTG
ENST00000444587.1:c.*184+59_*184+60delinsTG	ENSP00000488218.1:n.*184+59_*184+60delinsTG
ENST00000620888.4:c.315+59_315+60delinsTG	ENSP00000479637.1:n.315+59_315+60delinsTG
ENST00000624109.1:c.43-63_43-62delinsCA	ENSP00000485458.1:n.43-63_43-62delinsCA
NM_000184.2:c.315+59_315+60delinsTG	NP_000175.1:n.315+59_315+60delinsTG
NM_000184.3:c.315+59_315+60delinsTG MANE Select	NP_000175.1:n.315+59_315+60delinsTG