Canonical Allele Identifier: CA2838191271
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080256G>T , CM000670.2:g.127080256G>T GRCh38
NC_000008.10:g.128092501G>T , CM000670.1:g.128092501G>T GRCh37
NC_000008.9:g.128161683G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.383G>T (PRNCR1)
NR_119373.1:n.102-1123C>A (PCAT2)
Search 100 bp 5'
Search 100 bp 3'