Canonical Allele Identifier: CA1949577661

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254654_5254655delinsTC , CM000673.2:g.5254654_5254655delinsTC	GRCh38
NC_000011.9:g.5275884_5275885delinsTC , CM000673.1:g.5275884_5275885delinsTC	GRCh37
NC_000011.8:g.5232460_5232461delinsTC	NCBI36
NG_000007.3:g.42961_42962delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.74_75delinsGA MANE Select	ENSP00000338082.4:p.Gly25=
ENST00000380252.6:c.-73-141_-73-140delinsGA	ENSP00000369602.2:n.-73-141_-73-140delinsGA
ENST00000380259.7:c.1620_1621delinsGA	ENSP00000369609.3:n.1620_1621delinsGA
ENST00000642908.1:c.74_75delinsGA	ENSP00000495346.1:p.Gly25=
ENST00000647543.1:c.74_75delinsGA	ENSP00000496470.1:p.Gly25=
ENST00000336906.4:c.74_75delinsGA	ENSP00000338082.4:p.Gly25=
ENST00000380252.5:c.63-141_63-140delinsGA	ENSP00000369602.1:n.63-141_63-140delinsGA
ENST00000380259.6:c.74_75delinsGA	ENSP00000369609.2:p.Gly25=
ENST00000444587.1:c.54+20_54+21delinsGA	ENSP00000488218.1:n.54+20_54+21delinsGA
ENST00000620888.4:c.74_75delinsGA	ENSP00000479637.1:p.Gly25=
ENST00000624109.1:c.283_284delinsTC	ENSP00000485458.1:p.Ser95=
NM_000184.2:c.74_75delinsGA	NP_000175.1:p.Gly25=
NM_000184.3:c.74_75delinsGA MANE Select	NP_000175.1:p.Gly25=