Canonical Allele Identifier: CA2638215012

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374952-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374956dup , CM000679.2:g.44374956dup	GRCh38
NC_000017.10:g.42452324dup , CM000679.1:g.42452324dup	GRCh37
NC_000017.9:g.39807850dup	NCBI36
NG_008331.1:g.19553dup , LRG_479:g.19553dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+45dup MANE Select	ENSP00000262407.5:n.2841+45dup
ENST00000648408.1:c.2272+45dup
ENST00000262407.5:c.2841+45dup	ENSP00000262407.5:n.2841+45dup
ENST00000587295.5:c.253+880dup
ENST00000592462.5:n.2160dup
NM_000419.3:c.2841+45dup , LRG_479t1:c.2841+45dup	NP_000410.2:n.2841+45dup
XM_011524749.1:c.2841+45dup	XP_011523051.1:n.2841+45dup
XM_011524750.1:c.2841+45dup	XP_011523052.1:n.2841+45dup
NM_000419.4:c.2841+45dup	NP_000410.2:n.2841+45dup
NM_000419.5:c.2841+45dup MANE Select	NP_000410.2:n.2841+45dup