Canonical Allele Identifier: CA2782128091
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080050G>C , CM000670.2:g.127080050G>C GRCh38
NC_000008.10:g.128092295G>C , CM000670.1:g.128092295G>C GRCh37
NC_000008.9:g.128161477G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.177G>C (PRNCR1)
NR_119373.1:n.102-917C>G (PCAT2)