Canonical Allele Identifier: CA1818225101
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813581294

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080062A>C , CM000670.2:g.127080062A>C GRCh38
NC_000008.10:g.128092307A>C , CM000670.1:g.128092307A>C GRCh37
NC_000008.9:g.128161489A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.189A>C (PRNCR1)
NR_119373.1:n.102-929T>G (PCAT2)