Canonical Allele Identifier: CA2261367752
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379666_44379676delinsGGCCTGTCCCT , CM000679.2:g.44379666_44379676delinsGGCCTGTCCCT GRCh38
NC_000017.10:g.42457034_42457044delinsGGCCTGTCCCT , CM000679.1:g.42457034_42457044delinsGGCCTGTCCCT GRCh37
NC_000017.9:g.39812560_39812570delinsGGCCTGTCCCT NCBI36
NG_008331.1:g.14830_14840delinsAGGGACAGGCC , LRG_479:g.14830_14840delinsAGGGACAGGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1878+13_1878+23delinsAGGGACAGGCC MANE Select ENSP00000262407.5:n.1878+13_1878+23delins...
ENST00000648408.1:c.1309+13_1309+23delinsAGGGACAGGCC
ENST00000262407.5:c.1878+13_1878+23delinsAGGGACAGGCC ENSP00000262407.5:n.1878+13_1878+23delins...
ENST00000592462.5:n.673+13_673+23delinsAGGGACAGGCC
NM_000419.3:c.1878+13_1878+23delinsAGGGACAGGCC , LRG_479t1:c.1878+13_1878+23delinsAGGGACAGGCC NP_000410.2:n.1878+13_1878+23delinsAGGGAC...
XM_011524749.1:c.1878+13_1878+23delinsAGGGACAGGCC XP_011523051.1:n.1878+13_1878+23delinsAGG...
XM_011524750.1:c.1878+13_1878+23delinsAGGGACAGGCC XP_011523052.1:n.1878+13_1878+23delinsAGG...
NM_000419.4:c.1878+13_1878+23delinsAGGGACAGGCC NP_000410.2:n.1878+13_1878+23delinsAGGGAC...
NM_000419.5:c.1878+13_1878+23delinsAGGGACAGGCC MANE Select NP_000410.2:n.1878+13_1878+23delinsAGGGAC...