Canonical Allele Identifier: CA2638214982

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374926-ACCCCGCCCCTCCCAGAGCAAAGTGGTCCCCGCCCAGAAGGCCCGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374936_44374980del , CM000679.2:g.44374936_44374980del	GRCh38
NC_000017.10:g.42452304_42452348del , CM000679.1:g.42452304_42452348del	GRCh37
NC_000017.9:g.39807830_39807874del	NCBI36
NG_008331.1:g.19535_19579del , LRG_479:g.19535_19579del

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+27_2841+71del MANE Select	ENSP00000262407.5:n.2841+27_2841+71del
ENST00000648408.1:c.2272+27_2272+71del
ENST00000262407.5:c.2841+27_2841+71del	ENSP00000262407.5:n.2841+27_2841+71del
ENST00000587295.5:c.253+862_253+906del
ENST00000592462.5:n.2142_2186del
NM_000419.3:c.2841+27_2841+71del , LRG_479t1:c.2841+27_2841+71del	NP_000410.2:n.2841+27_2841+71del
XM_011524749.1:c.2841+27_2841+71del	XP_011523051.1:n.2841+27_2841+71del
XM_011524750.1:c.2841+27_2841+71del	XP_011523052.1:n.2841+27_2841+71del
NM_000419.4:c.2841+27_2841+71del	NP_000410.2:n.2841+27_2841+71del
NM_000419.5:c.2841+27_2841+71del MANE Select	NP_000410.2:n.2841+27_2841+71del