Canonical Allele Identifier: CA2638215411

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44375397-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375401_44375402del , CM000679.2:g.44375401_44375402del	GRCh38
NC_000017.10:g.42452769_42452770del , CM000679.1:g.42452769_42452770del	GRCh37
NC_000017.9:g.39808295_39808296del	NCBI36
NG_008331.1:g.19107_19108del , LRG_479:g.19107_19108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2727+192_2727+193del MANE Select	ENSP00000262407.5:n.2727+192_2727+193del
ENST00000648408.1:c.2158+192_2158+193del
ENST00000262407.5:c.2727+192_2727+193del	ENSP00000262407.5:n.2727+192_2727+193del
ENST00000587295.5:c.253+434_253+435del
ENST00000592462.5:n.1714_1715del
NM_000419.3:c.2727+192_2727+193del , LRG_479t1:c.2727+192_2727+193del	NP_000410.2:n.2727+192_2727+193del
XM_011524749.1:c.2727+192_2727+193del	XP_011523051.1:n.2727+192_2727+193del
XM_011524750.1:c.2727+192_2727+193del	XP_011523052.1:n.2727+192_2727+193del
NM_000419.4:c.2727+192_2727+193del	NP_000410.2:n.2727+192_2727+193del
NM_000419.5:c.2727+192_2727+193del MANE Select	NP_000410.2:n.2727+192_2727+193del