Canonical Allele Identifier: CA2688533353
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080234G>T , CM000670.2:g.127080234G>T GRCh38
NC_000008.10:g.128092479G>T , CM000670.1:g.128092479G>T GRCh37
NC_000008.9:g.128161661G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.361G>T (PRNCR1)
NR_119373.1:n.102-1101C>A (PCAT2)