Canonical Allele Identifier: CA12505798
Gene: PPIA HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.44796669C>G
GRCh37 chr7:g.44836268C>G
gnomAD v2:
7:44836268 C / G
gnomAD v3:
7:44796669 C / G
gnomAD v4:
chr7-44796669-C-G
Joint Max Group AF 0.07746706 (NFE)
Genomes Max Group AF 0.07268423 (AMR)
Exomes Max Group AF 0.07791416 (NFE)
dbSNP:
8177826
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44796669C>G , CM000669.2:g.44796669C>G GRCh38
NC_000007.13:g.44836268C>G , CM000669.1:g.44836268C>G GRCh37
NC_000007.12:g.44802793C>G NCBI36
NG_029697.1:g.5028C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001300981.1:c.-393C>G NP_001287910.1:n.-393C>G
NM_021130.4:c.-56C>G NP_066953.1:n.-56C>G
XR_002956460.1:n.710C>G
Search 100 bp 5'
Search 100 bp 3'