Canonical Allele Identifier: CA15551158
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.127081052C>T
GRCh37 chr8:g.128093297C>T
gnomAD v2:
8:128093297 C / T
gnomAD v3:
8:127081052 C / T
gnomAD v4:
chr8-127081052-C-T
Joint Max Group AF 0.31422847 (EAS)
Genomes Max Group AF 0.31435008 (EAS)
Exomes Max Group AF 0.02725563 (NFE)
dbSNP:
1016343
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127081052C>T , CM000670.2:g.127081052C>T GRCh38
NC_000008.10:g.128093297C>T , CM000670.1:g.128093297C>T GRCh37
NC_000008.9:g.128162479C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.1179C>T (PRNCR1)
NR_119373.1:n.101+1069G>A (PCAT2)
Search 100 bp 5'
Search 100 bp 3'