Canonical Allele Identifier: CA290942575
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs577209460

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372233T>C , CM000679.2:g.44372233T>C GRCh38
NC_000017.10:g.42449601T>C , CM000679.1:g.42449601T>C GRCh37
NC_000017.9:g.39805127T>C NCBI36
NG_008331.1:g.22273A>G , LRG_479:g.22273A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*131A>G MANE Select ENSP00000262407.5:n.*131A>G
ENST00000648408.1:c.2565A>G
ENST00000262407.5:c.*131A>G ENSP00000262407.5:n.*131A>G
ENST00000587295.5:c.444A>G
ENST00000588098.1:c.228A>G
NM_000419.3:c.*131A>G , LRG_479t1:c.*131A>G NP_000410.2:n.*131A>G
XM_011524749.1:c.*131A>G XP_011523051.1:n.*131A>G
XM_011524750.1:c.*131A>G XP_011523052.1:n.*131A>G
NM_000419.4:c.*131A>G NP_000410.2:n.*131A>G
NM_000419.5:c.*131A>G MANE Select NP_000410.2:n.*131A>G