Canonical Allele Identifier: CA1818224959
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079879T= , CM000670.2:g.127079879T= GRCh38
NC_000008.10:g.128092124T= , CM000670.1:g.128092124T= GRCh37
NC_000008.9:g.128161306T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.6T= (PRNCR1)
NR_119373.1:n.102-746A= (PCAT2)