Canonical Allele Identifier: CA2536303200
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080263G>C , CM000670.2:g.127080263G>C GRCh38
NC_000008.10:g.128092508G>C , CM000670.1:g.128092508G>C GRCh37
NC_000008.9:g.128161690G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.390G>C (PRNCR1)
NR_119373.1:n.102-1130C>G (PCAT2)