Canonical Allele Identifier: CA1818225412
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813588570
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080355G>C , CM000670.2:g.127080355G>C GRCh38
NC_000008.10:g.128092600G>C , CM000670.1:g.128092600G>C GRCh37
NC_000008.9:g.128161782G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.482G>C (PRNCR1)
NR_119373.1:n.102-1222C>G (PCAT2)
Search 100 bp 5'
Search 100 bp 3'