Canonical Allele Identifier: CA271416320
Gene: PPIB HGNC NCBI

Linked Data

dbSNP Id: rs890075179

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162934A>G , CM000677.2:g.64162934A>G GRCh38
NC_000015.9:g.64455133A>G , CM000677.1:g.64455133A>G GRCh37
NC_000015.8:g.62242186A>G NCBI36
NG_012979.1:g.5222T>C , LRG_10:g.5222T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.53T>C MANE Select ENSP00000300026.4:p.Ile18Thr
ENST00000561048.2:n.86T>C
ENST00000680158.1:c.53T>C ENSP00000504873.1:p.Ile18Thr
ENST00000681397.1:c.53T>C ENSP00000506584.1:p.Ile18Thr
ENST00000681658.1:c.30+23T>C ENSP00000505431.1:n.30+23T>C
ENST00000300026.3:c.53T>C ENSP00000300026.3:p.Ile18Thr
ENST00000558492.1:n.73T>C
ENST00000561048.1:n.88T>C
NM_000942.4:c.53T>C , LRG_10t1:c.53T>C NP_000933.1:p.Ile18Thr
NM_000942.5:c.53T>C MANE Select NP_000933.1:p.Ile18Thr