Canonical Allele Identifier: CA2688533351
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080223C>A , CM000670.2:g.127080223C>A GRCh38
NC_000008.10:g.128092468C>A , CM000670.1:g.128092468C>A GRCh37
NC_000008.9:g.128161650C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.350C>A (PRNCR1)
NR_119373.1:n.102-1090G>T (PCAT2)