Canonical Allele Identifier: CA7608531
Gene: PPIB HGNC NCBI

Linked Data

dbSNP Id: rs199971446

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64160109G>A , CM000677.2:g.64160109G>A GRCh38
NC_000015.9:g.64452308G>A , CM000677.1:g.64452308G>A GRCh37
NC_000015.8:g.62239361G>A NCBI36
NG_012979.1:g.8047C>T , LRG_10:g.8047C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.338C>T MANE Select ENSP00000300026.4:p.Thr113Ile
ENST00000561048.2:n.371C>T
ENST00000680158.1:c.338C>T ENSP00000504873.1:p.Thr113Ile
ENST00000680343.1:n.292C>T
ENST00000681397.1:c.338C>T ENSP00000506584.1:p.Thr113Ile
ENST00000681658.1:c.233C>T ENSP00000505431.1:p.Thr78Ile
ENST00000300026.3:c.338C>T ENSP00000300026.3:p.Thr113Ile
ENST00000558492.1:n.244C>T
ENST00000561048.1:n.373C>T
NM_000942.4:c.338C>T , LRG_10t1:c.338C>T NP_000933.1:p.Thr113Ile
NM_000942.5:c.338C>T MANE Select NP_000933.1:p.Thr113Ile