Canonical Allele Identifier: CA2688533271
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079968G>T , CM000670.2:g.127079968G>T GRCh38
NC_000008.10:g.128092213G>T , CM000670.1:g.128092213G>T GRCh37
NC_000008.9:g.128161395G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.95G>T (PRNCR1)
NR_119373.1:n.102-835C>A (PCAT2)