Canonical Allele Identifier: CA2638217431
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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