Canonical Allele Identifier: CA2511954070
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080299C>T , CM000670.2:g.127080299C>T GRCh38
NC_000008.10:g.128092544C>T , CM000670.1:g.128092544C>T GRCh37
NC_000008.9:g.128161726C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.426C>T (PRNCR1)
NR_119373.1:n.102-1166G>A (PCAT2)