Canonical Allele Identifier: CA10646410
Gene: PPIB HGNC NCBI

Linked Data

ClinVar Variation Id: 316711
ClinVar RCV Id: RCV000291583
dbSNP Id: rs886051327

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64163104T>C , CM000677.2:g.64163104T>C GRCh38
NC_000015.9:g.64455303T>C , CM000677.1:g.64455303T>C GRCh37
NC_000015.8:g.62242356T>C NCBI36
NG_012979.1:g.5052A>G , LRG_10:g.5052A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680158.1:c.-118A>G ENSP00000504873.1:n.-118A>G
ENST00000300026.3:c.-118A>G ENSP00000300026.3:n.-118A>G
NM_000942.4:c.-118A>G , LRG_10t1:c.-118A>G NP_000933.1:n.-118A>G