Canonical Allele Identifier: CA399787966
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs755197006

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372423C>T , CM000679.2:g.44372423C>T GRCh38
NC_000017.10:g.42449791C>T , CM000679.1:g.42449791C>T GRCh37
NC_000017.9:g.39805317C>T NCBI36
NG_008331.1:g.22083G>A , LRG_479:g.22083G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061G>A MANE Select ENSP00000262407.5:p.Val1021Ile
ENST00000648408.1:c.2375G>A
ENST00000262407.5:c.3061G>A ENSP00000262407.5:p.Val1021Ile
ENST00000587295.5:c.254G>A
ENST00000588098.1:c.38G>A
NM_000419.3:c.3061G>A , LRG_479t1:c.3061G>A NP_000410.2:p.Val1021Ile
XM_011524749.1:c.2959G>A XP_011523051.1:p.Val987Ile
XM_011524750.1:c.2944G>A XP_011523052.1:p.Val982Ile
NM_000419.4:c.3061G>A NP_000410.2:p.Val1021Ile
NM_000419.5:c.3061G>A MANE Select NP_000410.2:p.Val1021Ile