Canonical Allele Identifier: CA847138944
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1157947105

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080149G>A , CM000670.2:g.127080149G>A GRCh38
NC_000008.10:g.128092394G>A , CM000670.1:g.128092394G>A GRCh37
NC_000008.9:g.128161576G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.276G>A (PRNCR1)
NR_119373.1:n.102-1016C>T (PCAT2)