Canonical Allele Identifier: CA970721276
Gene: PPIB HGNC NCBI

Linked Data

dbSNP Id: rs2081569846

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162773G>A , CM000677.2:g.64162773G>A GRCh38
NC_000015.9:g.64454972G>A , CM000677.1:g.64454972G>A GRCh37
NC_000015.8:g.62242025G>A NCBI36
NG_012979.1:g.5383C>T , LRG_10:g.5383C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.135+79C>T MANE Select ENSP00000300026.4:n.135+79C>T
ENST00000561048.2:n.168+79C>T
ENST00000680158.1:c.135+79C>T ENSP00000504873.1:n.135+79C>T
ENST00000681397.1:c.135+79C>T ENSP00000506584.1:n.135+79C>T
ENST00000681658.1:c.30+184C>T ENSP00000505431.1:n.30+184C>T
ENST00000300026.3:c.135+79C>T ENSP00000300026.3:n.135+79C>T
ENST00000558492.1:n.155+79C>T
ENST00000561048.1:n.170+79C>T
NM_000942.4:c.135+79C>T , LRG_10t1:c.135+79C>T NP_000933.1:n.135+79C>T
NM_000942.5:c.135+79C>T MANE Select NP_000933.1:n.135+79C>T