Canonical Allele Identifier: CA8603382

Gene: ITGA2B

Linked Data

• dbSNP Id: rs748572066
• ExAC: 17:42462482 G / T
• gnomAD v2: 17-42462482-G-T
• gnomAD v3: 17-44385114-G-T
• gnomAD v4: 17-44385114-G-T
• MyVariant Identifiers: chr17:g.42462482G>T (hg19) ; chr17:g.44385114G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385114G>T , CM000679.2:g.44385114G>T	GRCh38
NC_000017.10:g.42462482G>T , CM000679.1:g.42462482G>T	GRCh37
NC_000017.9:g.39818008G>T	NCBI36
NG_008331.1:g.9392C>A , LRG_479:g.9392C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.671-38C>A MANE Select	ENSP00000262407.5:n.671-38C>A
ENST00000648408.1:c.102-38C>A
ENST00000262407.5:c.671-38C>A	ENSP00000262407.5:n.671-38C>A
ENST00000589645.5:n.122-38C>A
ENST00000591990.5:n.33-38C>A
ENST00000592075.5:n.40-38C>A
ENST00000592226.5:n.39+50C>A
ENST00000592253.5:n.179-38C>A
ENST00000592944.1:n.353-38C>A
NM_000419.3:c.671-38C>A , LRG_479t1:c.671-38C>A	NP_000410.2:n.671-38C>A
XM_011524749.1:c.671-38C>A	XP_011523051.1:n.671-38C>A
XM_011524750.1:c.671-38C>A	XP_011523052.1:n.671-38C>A
NM_000419.4:c.671-38C>A	NP_000410.2:n.671-38C>A
NM_000419.5:c.671-38C>A MANE Select	NP_000410.2:n.671-38C>A