Canonical Allele Identifier: CA2638215124

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44375085-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375085_44375086insCT , CM000679.2:g.44375085_44375086insCT	GRCh38
NC_000017.10:g.42452453_42452454insCT , CM000679.1:g.42452453_42452454insCT	GRCh37
NC_000017.9:g.39807979_39807980insCT	NCBI36
NG_008331.1:g.19420_19421insAG , LRG_479:g.19420_19421insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2753_2754insAG MANE Select	ENSP00000262407.5:p.Val919GlyfsTer?
ENST00000648408.1:c.2184_2185insAG
ENST00000262407.5:c.2753_2754insAG	ENSP00000262407.5:p.Val919GlyfsTer?
ENST00000587295.5:c.253+747_253+748insAG
ENST00000592462.5:n.2027_2028insAG
NM_000419.3:c.2753_2754insAG , LRG_479t1:c.2753_2754insAG	NP_000410.2:p.Val919GlyfsTer?
XM_011524749.1:c.2753_2754insAG	XP_011523051.1:p.Val919GlyfsTer?
XM_011524750.1:c.2753_2754insAG	XP_011523052.1:p.Val919GlyfsTer?
NM_000419.4:c.2753_2754insAG	NP_000410.2:p.Val919GlyfsTer?
NM_000419.5:c.2753_2754insAG MANE Select	NP_000410.2:p.Val919GlyfsTer?