Canonical Allele Identifier: CA2514754620

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374953_44374960dup , CM000679.2:g.44374953_44374960dup	GRCh38
NC_000017.10:g.42452321_42452328dup , CM000679.1:g.42452321_42452328dup	GRCh37
NC_000017.9:g.39807847_39807854dup	NCBI36
NG_008331.1:g.19546_19553dup , LRG_479:g.19546_19553dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+38_2841+45dup MANE Select	ENSP00000262407.5:n.2841+38_2841+45dup
ENST00000648408.1:c.2272+38_2272+45dup
ENST00000262407.5:c.2841+38_2841+45dup	ENSP00000262407.5:n.2841+38_2841+45dup
ENST00000587295.5:c.253+873_253+880dup
ENST00000592462.5:n.2153_2160dup
NM_000419.3:c.2841+38_2841+45dup , LRG_479t1:c.2841+38_2841+45dup	NP_000410.2:n.2841+38_2841+45dup
XM_011524749.1:c.2841+38_2841+45dup	XP_011523051.1:n.2841+38_2841+45dup
XM_011524750.1:c.2841+38_2841+45dup	XP_011523052.1:n.2841+38_2841+45dup
NM_000419.4:c.2841+38_2841+45dup	NP_000410.2:n.2841+38_2841+45dup
NM_000419.5:c.2841+38_2841+45dup MANE Select	NP_000410.2:n.2841+38_2841+45dup