Canonical Allele Identifier: CA2638213291
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372235G>T , CM000679.2:g.44372235G>T GRCh38
NC_000017.10:g.42449603G>T , CM000679.1:g.42449603G>T GRCh37
NC_000017.9:g.39805129G>T NCBI36
NG_008331.1:g.22271C>A , LRG_479:g.22271C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*129C>A MANE Select ENSP00000262407.5:n.*129C>A
ENST00000648408.1:c.2563C>A
ENST00000262407.5:c.*129C>A ENSP00000262407.5:n.*129C>A
ENST00000587295.5:c.442C>A
ENST00000588098.1:c.226C>A
NM_000419.3:c.*129C>A , LRG_479t1:c.*129C>A NP_000410.2:n.*129C>A
XM_011524749.1:c.*129C>A XP_011523051.1:n.*129C>A
XM_011524750.1:c.*129C>A XP_011523052.1:n.*129C>A
NM_000419.4:c.*129C>A NP_000410.2:n.*129C>A
NM_000419.5:c.*129C>A MANE Select NP_000410.2:n.*129C>A