Canonical Allele Identifier: CA2790279870

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254663_5254664del , CM000673.2:g.5254663_5254664del	GRCh38
NC_000011.9:g.5275893_5275894del , CM000673.1:g.5275893_5275894del	GRCh37
NC_000011.8:g.5232469_5232470del	NCBI36
NG_000007.3:g.42952_42953del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.65_66del MANE Select	ENSP00000338082.4:p.Glu22GlyfsTer22
ENST00000380252.6:c.-73-150_-73-149del	ENSP00000369602.2:n.-73-150_-73-149del
ENST00000380259.7:c.1611_1612del	ENSP00000369609.3:n.1611_1612del
ENST00000642908.1:c.65_66del	ENSP00000495346.1:p.Glu22GlyfsTer22
ENST00000647543.1:c.65_66del	ENSP00000496470.1:p.Glu22GlyfsTer22
ENST00000336906.4:c.65_66del	ENSP00000338082.4:p.Glu22GlyfsTer22
ENST00000380252.5:c.63-150_63-149del	ENSP00000369602.1:n.63-150_63-149del
ENST00000380259.6:c.65_66del	ENSP00000369609.2:p.Glu22GlyfsTer22
ENST00000444587.1:c.54+11_54+12del	ENSP00000488218.1:n.54+11_54+12del
ENST00000620888.4:c.65_66del	ENSP00000479637.1:p.Glu22GlyfsTer22
ENST00000624109.1:c.292_293del	ENSP00000485458.1:p.Phe98ProfsTer10
NM_000184.2:c.65_66del	NP_000175.1:p.Glu22GlyfsTer22
NM_000184.3:c.65_66del MANE Select	NP_000175.1:p.Glu22GlyfsTer22