Canonical Allele Identifier: CA2261367720
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379561_44379562delinsGA , CM000679.2:g.44379561_44379562delinsGA GRCh38
NC_000017.10:g.42456929_42456930delinsGA , CM000679.1:g.42456929_42456930delinsGA GRCh37
NC_000017.9:g.39812455_39812456delinsGA NCBI36
NG_008331.1:g.14944_14945delinsTC , LRG_479:g.14944_14945delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1878+127_1878+128delinsTC MANE Select ENSP00000262407.5:n.1878+127_1878+128deli...
ENST00000648408.1:c.1309+127_1309+128delinsTC
ENST00000262407.5:c.1878+127_1878+128delinsTC ENSP00000262407.5:n.1878+127_1878+128deli...
ENST00000592462.5:n.673+127_673+128delinsTC
NM_000419.3:c.1878+127_1878+128delinsTC , LRG_479t1:c.1878+127_1878+128delinsTC NP_000410.2:n.1878+127_1878+128delinsTC
XM_011524749.1:c.1878+127_1878+128delinsTC XP_011523051.1:n.1878+127_1878+128delinsT...
XM_011524750.1:c.1878+127_1878+128delinsTC XP_011523052.1:n.1878+127_1878+128delinsT...
NM_000419.4:c.1878+127_1878+128delinsTC NP_000410.2:n.1878+127_1878+128delinsTC
NM_000419.5:c.1878+127_1878+128delinsTC MANE Select NP_000410.2:n.1878+127_1878+128delinsTC