Canonical Allele Identifier: CA1818225341
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080297A= , CM000670.2:g.127080297A= GRCh38
NC_000008.10:g.128092542A= , CM000670.1:g.128092542A= GRCh37
NC_000008.9:g.128161724A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.424A= (PRNCR1)
NR_119373.1:n.102-1164T= (PCAT2)