Canonical Allele Identifier: CA2638214986

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374931-GCCCCTCCCAGAGCAAAGTGGTCCCCGCCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374932_44374961del , CM000679.2:g.44374932_44374961del	GRCh38
NC_000017.10:g.42452300_42452329del , CM000679.1:g.42452300_42452329del	GRCh37
NC_000017.9:g.39807826_39807855del	NCBI36
NG_008331.1:g.19545_19574del , LRG_479:g.19545_19574del

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+37_2841+66del MANE Select	ENSP00000262407.5:n.2841+37_2841+66del
ENST00000648408.1:c.2272+37_2272+66del
ENST00000262407.5:c.2841+37_2841+66del	ENSP00000262407.5:n.2841+37_2841+66del
ENST00000587295.5:c.253+872_253+901del
ENST00000592462.5:n.2152_2181del
NM_000419.3:c.2841+37_2841+66del , LRG_479t1:c.2841+37_2841+66del	NP_000410.2:n.2841+37_2841+66del
XM_011524749.1:c.2841+37_2841+66del	XP_011523051.1:n.2841+37_2841+66del
XM_011524750.1:c.2841+37_2841+66del	XP_011523052.1:n.2841+37_2841+66del
NM_000419.4:c.2841+37_2841+66del	NP_000410.2:n.2841+37_2841+66del
NM_000419.5:c.2841+37_2841+66del MANE Select	NP_000410.2:n.2841+37_2841+66del