Canonical Allele Identifier: CA1818224992
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079912A= , CM000670.2:g.127079912A= GRCh38
NC_000008.10:g.128092157A= , CM000670.1:g.128092157A= GRCh37
NC_000008.9:g.128161339A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.39A= (PRNCR1)
NR_119373.1:n.102-779T= (PCAT2)