Canonical Allele Identifier: CA772288639
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs1319569835

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379598del , CM000679.2:g.44379598del GRCh38
NC_000017.10:g.42456966del , CM000679.1:g.42456966del GRCh37
NC_000017.9:g.39812492del NCBI36
NG_008331.1:g.14911del , LRG_479:g.14911del

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1878+94del MANE Select ENSP00000262407.5:n.1878+94del
ENST00000648408.1:c.1309+94del
ENST00000262407.5:c.1878+94del ENSP00000262407.5:n.1878+94del
ENST00000592462.5:n.673+94del
NM_000419.3:c.1878+94del , LRG_479t1:c.1878+94del NP_000410.2:n.1878+94del
XM_011524749.1:c.1878+94del XP_011523051.1:n.1878+94del
XM_011524750.1:c.1878+94del XP_011523052.1:n.1878+94del
NM_000419.4:c.1878+94del NP_000410.2:n.1878+94del
NM_000419.5:c.1878+94del MANE Select NP_000410.2:n.1878+94del