Canonical Allele Identifier: CA2688533589
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs940375362
gnomAD v4: 8-127081062-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127081062T>C , CM000670.2:g.127081062T>C GRCh38
NC_000008.10:g.128093307T>C , CM000670.1:g.128093307T>C GRCh37
NC_000008.9:g.128162489T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.1189T>C (PRNCR1)
NR_119373.1:n.101+1059A>G (PCAT2)
Search 100 bp 5'
Search 100 bp 3'