Canonical Allele Identifier: CA2612152528

Gene: HBG2

Linked Data

• gnomAD v4: 11-5254597-GTCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254605_5254608del , CM000673.2:g.5254605_5254608del	GRCh38
NC_000011.9:g.5275835_5275838del , CM000673.1:g.5275835_5275838del	GRCh37
NC_000011.8:g.5232411_5232414del	NCBI36
NG_000007.3:g.43015_43018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.92+36_92+39del MANE Select	ENSP00000338082.4:n.92+36_92+39del
ENST00000380252.6:c.-73-87_-73-84del	ENSP00000369602.2:n.-73-87_-73-84del
ENST00000380259.7:c.1638+36_1638+39del	ENSP00000369609.3:n.1638+36_1638+39del
ENST00000642908.1:c.92+36_92+39del	ENSP00000495346.1:n.92+36_92+39del
ENST00000647543.1:c.92+36_92+39del	ENSP00000496470.1:n.92+36_92+39del
ENST00000336906.4:c.92+36_92+39del	ENSP00000338082.4:n.92+36_92+39del
ENST00000380252.5:c.63-87_63-84del	ENSP00000369602.1:n.63-87_63-84del
ENST00000380259.6:c.92+36_92+39del	ENSP00000369609.2:n.92+36_92+39del
ENST00000444587.1:c.54+74_54+77del	ENSP00000488218.1:n.54+74_54+77del
ENST00000620888.4:c.92+36_92+39del	ENSP00000479637.1:n.92+36_92+39del
ENST00000624109.1:c.265-31_265-28del	ENSP00000485458.1:n.265-31_265-28del
NM_000184.2:c.92+36_92+39del	NP_000175.1:n.92+36_92+39del
NM_000184.3:c.92+36_92+39del MANE Select	NP_000175.1:n.92+36_92+39del