Canonical Allele Identifier: CA2612152554

Gene: HBG2

Linked Data

• gnomAD v4: 11-5254649-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254654_5254656del , CM000673.2:g.5254654_5254656del	GRCh38
NC_000011.9:g.5275884_5275886del , CM000673.1:g.5275884_5275886del	GRCh37
NC_000011.8:g.5232460_5232462del	NCBI36
NG_000007.3:g.42964_42966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.77_79del MANE Select	ENSP00000338082.4:p.Gly26del
ENST00000380252.6:c.-73-138_-73-136del	ENSP00000369602.2:n.-73-138_-73-136del
ENST00000380259.7:c.1623_1625del	ENSP00000369609.3:n.1623_1625del
ENST00000642908.1:c.77_79del	ENSP00000495346.1:p.Gly26del
ENST00000647543.1:c.77_79del	ENSP00000496470.1:p.Gly26del
ENST00000336906.4:c.77_79del	ENSP00000338082.4:p.Gly26del
ENST00000380252.5:c.63-138_63-136del	ENSP00000369602.1:n.63-138_63-136del
ENST00000380259.6:c.77_79del	ENSP00000369609.2:p.Gly26del
ENST00000444587.1:c.54+23_54+25del	ENSP00000488218.1:n.54+23_54+25del
ENST00000620888.4:c.77_79del	ENSP00000479637.1:p.Gly26del
ENST00000624109.1:c.283_285del	ENSP00000485458.1:p.Ser95del
NM_000184.2:c.77_79del	NP_000175.1:p.Gly26del
NM_000184.3:c.77_79del MANE Select	NP_000175.1:p.Gly26del