Canonical Allele Identifier: CA10575572
Gene: ITGA2B HGNC NCBI

Linked Data

ClinVar Variation Id: 50232
dbSNP Id: rs879255514

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372407C>T , CM000679.2:g.44372407C>T GRCh38
NC_000017.10:g.42449775C>T , CM000679.1:g.42449775C>T GRCh37
NC_000017.9:g.39805301C>T NCBI36
NG_008331.1:g.22099G>A , LRG_479:g.22099G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3077G>A MANE Select ENSP00000262407.5:p.Arg1026Gln
ENST00000648408.1:c.2391G>A
ENST00000262407.5:c.3077G>A ENSP00000262407.5:p.Arg1026Gln
ENST00000587295.5:c.270G>A
ENST00000588098.1:c.54G>A
NM_000419.3:c.3077G>A , LRG_479t1:c.3077G>A NP_000410.2:p.Arg1026Gln
XM_011524749.1:c.2975G>A XP_011523051.1:p.Arg992Gln
XM_011524750.1:c.2960G>A XP_011523052.1:p.Arg987Gln
NM_000419.4:c.3077G>A NP_000410.2:p.Arg1026Gln
NM_000419.5:c.3077G>A MANE Select NP_000410.2:p.Arg1026Gln