Canonical Allele Identifier: CA2638215529

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44375547-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375550del , CM000679.2:g.44375550del	GRCh38
NC_000017.10:g.42452918del , CM000679.1:g.42452918del	GRCh37
NC_000017.9:g.39808444del	NCBI36
NG_008331.1:g.18958del , LRG_479:g.18958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2727+43del MANE Select	ENSP00000262407.5:n.2727+43del
ENST00000648408.1:c.2158+43del
ENST00000262407.5:c.2727+43del	ENSP00000262407.5:n.2727+43del
ENST00000587295.5:c.253+285del
ENST00000592462.5:n.1565del
NM_000419.3:c.2727+43del , LRG_479t1:c.2727+43del	NP_000410.2:n.2727+43del
XM_011524749.1:c.2727+43del	XP_011523051.1:n.2727+43del
XM_011524750.1:c.2727+43del	XP_011523052.1:n.2727+43del
NM_000419.4:c.2727+43del	NP_000410.2:n.2727+43del
NM_000419.5:c.2727+43del MANE Select	NP_000410.2:n.2727+43del