Canonical Allele Identifier: CA2261367728
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379594_44379595delinsGT , CM000679.2:g.44379594_44379595delinsGT GRCh38
NC_000017.10:g.42456962_42456963delinsGT , CM000679.1:g.42456962_42456963delinsGT GRCh37
NC_000017.9:g.39812488_39812489delinsGT NCBI36
NG_008331.1:g.14911_14912delinsAC , LRG_479:g.14911_14912delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1878+94_1878+95delinsAC MANE Select ENSP00000262407.5:n.1878+94_1878+95delins...
ENST00000648408.1:c.1309+94_1309+95delinsAC
ENST00000262407.5:c.1878+94_1878+95delinsAC ENSP00000262407.5:n.1878+94_1878+95delins...
ENST00000592462.5:n.673+94_673+95delinsAC
NM_000419.3:c.1878+94_1878+95delinsAC , LRG_479t1:c.1878+94_1878+95delinsAC NP_000410.2:n.1878+94_1878+95delinsAC
XM_011524749.1:c.1878+94_1878+95delinsAC XP_011523051.1:n.1878+94_1878+95delinsAC
XM_011524750.1:c.1878+94_1878+95delinsAC XP_011523052.1:n.1878+94_1878+95delinsAC
NM_000419.4:c.1878+94_1878+95delinsAC NP_000410.2:n.1878+94_1878+95delinsAC
NM_000419.5:c.1878+94_1878+95delinsAC MANE Select NP_000410.2:n.1878+94_1878+95delinsAC