Canonical Allele Identifier: CA2261365913
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375718_44375719delinsTG , CM000679.2:g.44375718_44375719delinsTG GRCh38
NC_000017.10:g.42453086_42453087delinsTG , CM000679.1:g.42453086_42453087delinsTG GRCh37
NC_000017.9:g.39808612_39808613delinsTG NCBI36
NG_008331.1:g.18787_18788delinsCA , LRG_479:g.18787_18788delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2602-3_2602-2delinsCA MANE Select ENSP00000262407.5:n.2602-3_2602-2delinsCA
ENST00000648408.1:c.2033-3_2033-2delinsCA
ENST00000262407.5:c.2602-3_2602-2delinsCA ENSP00000262407.5:n.2602-3_2602-2delinsCA
ENST00000587295.5:c.253+114_253+115delinsCA
ENST00000592462.5:n.1397-3_1397-2delinsCA
NM_000419.3:c.2602-3_2602-2delinsCA , LRG_479t1:c.2602-3_2602-2delinsCA NP_000410.2:n.2602-3_2602-2delinsCA
XM_011524749.1:c.2602-3_2602-2delinsCA XP_011523051.1:n.2602-3_2602-2delinsCA
XM_011524750.1:c.2602-3_2602-2delinsCA XP_011523052.1:n.2602-3_2602-2delinsCA
NM_000419.4:c.2602-3_2602-2delinsCA NP_000410.2:n.2602-3_2602-2delinsCA
NM_000419.5:c.2602-3_2602-2delinsCA MANE Select NP_000410.2:n.2602-3_2602-2delinsCA