Canonical Allele Identifier: CA1949577561

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254540_5254544delinsACAGT , CM000673.2:g.5254540_5254544delinsACAGT	GRCh38
NC_000011.9:g.5275770_5275774delinsACAGT , CM000673.1:g.5275770_5275774delinsACAGT	GRCh37
NC_000011.8:g.5232346_5232350delinsACAGT	NCBI36
NG_000007.3:g.43072_43076delinsACTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.93-30_93-26delinsACTGT MANE Select	ENSP00000338082.4:n.93-30_93-26delinsACTGT
ENST00000380252.6:c.-73-30_-73-26delinsACTGT	ENSP00000369602.2:n.-73-30_-73-26delinsACTGT
ENST00000380259.7:c.1639-30_1639-26delinsACTGT	ENSP00000369609.3:n.1639-30_1639-26delinsACTGT
ENST00000642908.1:c.93-30_93-26delinsACTGT	ENSP00000495346.1:n.93-30_93-26delinsACTGT
ENST00000647543.1:c.93-30_93-26delinsACTGT	ENSP00000496470.1:n.93-30_93-26delinsACTGT
ENST00000336906.4:c.93-30_93-26delinsACTGT	ENSP00000338082.4:n.93-30_93-26delinsACTGT
ENST00000380252.5:c.63-30_63-26delinsACTGT	ENSP00000369602.1:n.63-30_63-26delinsACTGT
ENST00000380259.6:c.93-30_93-26delinsACTGT	ENSP00000369609.2:n.93-30_93-26delinsACTGT
ENST00000444587.1:c.55-30_55-26delinsACTGT	ENSP00000488218.1:n.55-30_55-26delinsACTGT
ENST00000620888.4:c.93-30_93-26delinsACTGT	ENSP00000479637.1:n.93-30_93-26delinsACTGT
ENST00000624109.1:c.264+24_264+28delinsACAGT	ENSP00000485458.1:n.264+24_264+28delinsACAGT
NM_000184.2:c.93-30_93-26delinsACTGT	NP_000175.1:n.93-30_93-26delinsACTGT
NM_000184.3:c.93-30_93-26delinsACTGT MANE Select	NP_000175.1:n.93-30_93-26delinsACTGT