Canonical Allele Identifier: CA271415965
Gene: PPIB HGNC NCBI

Linked Data

dbSNP Id: rs1010717111
MyVariant Identifiers: chr15:g.64454978G>T (hg19) chr15:g.64162779G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162779G>T , CM000677.2:g.64162779G>T GRCh38
NC_000015.9:g.64454978G>T , CM000677.1:g.64454978G>T GRCh37
NC_000015.8:g.62242031G>T NCBI36
NG_012979.1:g.5377C>A , LRG_10:g.5377C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.135+73C>A MANE Select ENSP00000300026.4:n.135+73C>A
ENST00000561048.2:n.168+73C>A
ENST00000680158.1:c.135+73C>A ENSP00000504873.1:n.135+73C>A
ENST00000681397.1:c.135+73C>A ENSP00000506584.1:n.135+73C>A
ENST00000681658.1:c.30+178C>A ENSP00000505431.1:n.30+178C>A
ENST00000300026.3:c.135+73C>A ENSP00000300026.3:n.135+73C>A
ENST00000558492.1:n.155+73C>A
ENST00000561048.1:n.170+73C>A
NM_000942.4:c.135+73C>A , LRG_10t1:c.135+73C>A NP_000933.1:n.135+73C>A
NM_000942.5:c.135+73C>A MANE Select NP_000933.1:n.135+73C>A
Search 100 bp 5'
Search 100 bp 3'