Canonical Allele Identifier: CA1818226305
Community Standard Title: NC_000008.11:g.127081052C=
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127081052C= , CM000670.2:g.127081052C= GRCh38
NC_000008.10:g.128093297C= , CM000670.1:g.128093297C= GRCh37
NC_000008.9:g.128162479C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.1179C= (PRNCR1)
NR_119373.1:n.101+1069G= (PCAT2)