Canonical Allele Identifier: CA1818226319
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127081062T= , CM000670.2:g.127081062T= GRCh38
NC_000008.10:g.128093307T= , CM000670.1:g.128093307T= GRCh37
NC_000008.9:g.128162489T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.1189T= (PRNCR1)
NR_119373.1:n.101+1059A= (PCAT2)