Canonical Allele Identifier: CA1818225290
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080256G= , CM000670.2:g.127080256G= GRCh38
NC_000008.10:g.128092501G= , CM000670.1:g.128092501G= GRCh37
NC_000008.9:g.128161683G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.383G= (PRNCR1)
NR_119373.1:n.102-1123C= (PCAT2)