Canonical Allele Identifier: CA1818225015
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813579837

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079943T>G , CM000670.2:g.127079943T>G GRCh38
NC_000008.10:g.128092188T>G , CM000670.1:g.128092188T>G GRCh37
NC_000008.9:g.128161370T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.70T>G (PRNCR1)
NR_119373.1:n.102-810A>C (PCAT2)