Canonical Allele Identifier: CA772284870
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs1160599771

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372647dup , CM000679.2:g.44372647dup GRCh38
NC_000017.10:g.42450015dup , CM000679.1:g.42450015dup GRCh37
NC_000017.9:g.39805541dup NCBI36
NG_008331.1:g.21866dup , LRG_479:g.21866dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-217dup MANE Select ENSP00000262407.5:n.3061-217dup
ENST00000648408.1:c.2375-217dup
ENST00000262407.5:c.3061-217dup ENSP00000262407.5:n.3061-217dup
ENST00000587295.5:c.254-217dup
ENST00000588098.1:c.38-217dup
NM_000419.3:c.3061-217dup , LRG_479t1:c.3061-217dup NP_000410.2:n.3061-217dup
XM_011524749.1:c.2959-217dup XP_011523051.1:n.2959-217dup
XM_011524750.1:c.2944-217dup XP_011523052.1:n.2944-217dup
NM_000419.4:c.3061-217dup NP_000410.2:n.3061-217dup
NM_000419.5:c.3061-217dup MANE Select NP_000410.2:n.3061-217dup