Canonical Allele Identifier: CA2638214960

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374911-G-GCCCTCCCACACCAAACCCCGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374920_44374940dup , CM000679.2:g.44374920_44374940dup	GRCh38
NC_000017.10:g.42452288_42452308dup , CM000679.1:g.42452288_42452308dup	GRCh37
NC_000017.9:g.39807814_39807834dup	NCBI36
NG_008331.1:g.19574_19594dup , LRG_479:g.19574_19594dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+66_2841+86dup MANE Select	ENSP00000262407.5:n.2841+66_2841+86dup
ENST00000648408.1:c.2272+66_2272+86dup
ENST00000262407.5:c.2841+66_2841+86dup	ENSP00000262407.5:n.2841+66_2841+86dup
ENST00000587295.5:c.253+901_253+921dup
ENST00000592462.5:n.2181_2201dup
NM_000419.3:c.2841+66_2841+86dup , LRG_479t1:c.2841+66_2841+86dup	NP_000410.2:n.2841+66_2841+86dup
XM_011524749.1:c.2841+66_2841+86dup	XP_011523051.1:n.2841+66_2841+86dup
XM_011524750.1:c.2841+66_2841+86dup	XP_011523052.1:n.2841+66_2841+86dup
NM_000419.4:c.2841+66_2841+86dup	NP_000410.2:n.2841+66_2841+86dup
NM_000419.5:c.2841+66_2841+86dup MANE Select	NP_000410.2:n.2841+66_2841+86dup