Canonical Allele Identifier: CA2638214839

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374600-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374601del , CM000679.2:g.44374601del	GRCh38
NC_000017.10:g.42451969del , CM000679.1:g.42451969del	GRCh37
NC_000017.9:g.39807495del	NCBI36
NG_008331.1:g.19905del , LRG_479:g.19905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2943+58del MANE Select	ENSP00000262407.5:n.2943+58del
ENST00000648408.1:c.2374+58del
ENST00000262407.5:c.2943+58del	ENSP00000262407.5:n.2943+58del
ENST00000587295.5:c.253+1232del
ENST00000588098.1:c.37+58del
ENST00000592462.5:n.2512del
NM_000419.3:c.2943+58del , LRG_479t1:c.2943+58del	NP_000410.2:n.2943+58del
XM_011524749.1:c.2842-131del	XP_011523051.1:n.2842-131del
XM_011524750.1:c.2943+58del	XP_011523052.1:n.2943+58del
NM_000419.4:c.2943+58del	NP_000410.2:n.2943+58del
NM_000419.5:c.2943+58del MANE Select	NP_000410.2:n.2943+58del