Canonical Allele Identifier: CA772285525

Gene: ITGA2B

Linked Data

• dbSNP Id: rs1357464081
• gnomAD v3: 17-44374928-C-T
• gnomAD v4: 17-44374928-C-T
• MyVariant Identifiers: chr17:g.42452296C>T (hg19) ; chr17:g.44374928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374928C>T , CM000679.2:g.44374928C>T	GRCh38
NC_000017.10:g.42452296C>T , CM000679.1:g.42452296C>T	GRCh37
NC_000017.9:g.39807822C>T	NCBI36
NG_008331.1:g.19578G>A , LRG_479:g.19578G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+70G>A MANE Select	ENSP00000262407.5:n.2841+70G>A
ENST00000648408.1:c.2272+70G>A
ENST00000262407.5:c.2841+70G>A	ENSP00000262407.5:n.2841+70G>A
ENST00000587295.5:c.253+905G>A
ENST00000592462.5:n.2185G>A
NM_000419.3:c.2841+70G>A , LRG_479t1:c.2841+70G>A	NP_000410.2:n.2841+70G>A
XM_011524749.1:c.2841+70G>A	XP_011523051.1:n.2841+70G>A
XM_011524750.1:c.2841+70G>A	XP_011523052.1:n.2841+70G>A
NM_000419.4:c.2841+70G>A	NP_000410.2:n.2841+70G>A
NM_000419.5:c.2841+70G>A MANE Select	NP_000410.2:n.2841+70G>A