Canonical Allele Identifier: CA2638215000

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374943-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374943G>T , CM000679.2:g.44374943G>T	GRCh38
NC_000017.10:g.42452311G>T , CM000679.1:g.42452311G>T	GRCh37
NC_000017.9:g.39807837G>T	NCBI36
NG_008331.1:g.19563C>A , LRG_479:g.19563C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+55C>A MANE Select	ENSP00000262407.5:n.2841+55C>A
ENST00000648408.1:c.2272+55C>A
ENST00000262407.5:c.2841+55C>A	ENSP00000262407.5:n.2841+55C>A
ENST00000587295.5:c.253+890C>A
ENST00000592462.5:n.2170C>A
NM_000419.3:c.2841+55C>A , LRG_479t1:c.2841+55C>A	NP_000410.2:n.2841+55C>A
XM_011524749.1:c.2841+55C>A	XP_011523051.1:n.2841+55C>A
XM_011524750.1:c.2841+55C>A	XP_011523052.1:n.2841+55C>A
NM_000419.4:c.2841+55C>A	NP_000410.2:n.2841+55C>A
NM_000419.5:c.2841+55C>A MANE Select	NP_000410.2:n.2841+55C>A