Canonical Allele Identifier: CA2688533324
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080145A>G , CM000670.2:g.127080145A>G GRCh38
NC_000008.10:g.128092390A>G , CM000670.1:g.128092390A>G GRCh37
NC_000008.9:g.128161572A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.272A>G (PRNCR1)
NR_119373.1:n.102-1012T>C (PCAT2)