Canonical Allele Identifier: CA1949577621

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254625_5254626delinsAC , CM000673.2:g.5254625_5254626delinsAC	GRCh38
NC_000011.9:g.5275855_5275856delinsAC , CM000673.1:g.5275855_5275856delinsAC	GRCh37
NC_000011.8:g.5232431_5232432delinsAC	NCBI36
NG_000007.3:g.42990_42991delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.92+11_92+12delinsGT MANE Select	ENSP00000338082.4:n.92+11_92+12delinsGT
ENST00000380252.6:c.-73-112_-73-111delinsGT	ENSP00000369602.2:n.-73-112_-73-111delinsGT
ENST00000380259.7:c.1638+11_1638+12delinsGT	ENSP00000369609.3:n.1638+11_1638+12delinsGT
ENST00000642908.1:c.92+11_92+12delinsGT	ENSP00000495346.1:n.92+11_92+12delinsGT
ENST00000647543.1:c.92+11_92+12delinsGT	ENSP00000496470.1:n.92+11_92+12delinsGT
ENST00000336906.4:c.92+11_92+12delinsGT	ENSP00000338082.4:n.92+11_92+12delinsGT
ENST00000380252.5:c.63-112_63-111delinsGT	ENSP00000369602.1:n.63-112_63-111delinsGT
ENST00000380259.6:c.92+11_92+12delinsGT	ENSP00000369609.2:n.92+11_92+12delinsGT
ENST00000444587.1:c.54+49_54+50delinsGT	ENSP00000488218.1:n.54+49_54+50delinsGT
ENST00000620888.4:c.92+11_92+12delinsGT	ENSP00000479637.1:n.92+11_92+12delinsGT
ENST00000624109.1:c.265-11_265-10delinsAC	ENSP00000485458.1:n.265-11_265-10delinsAC
NM_000184.2:c.92+11_92+12delinsGT	NP_000175.1:n.92+11_92+12delinsGT
NM_000184.3:c.92+11_92+12delinsGT MANE Select	NP_000175.1:n.92+11_92+12delinsGT