Canonical Allele Identifier: CA2688533272
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079976G>A , CM000670.2:g.127079976G>A GRCh38
NC_000008.10:g.128092221G>A , CM000670.1:g.128092221G>A GRCh37
NC_000008.9:g.128161403G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.103G>A (PRNCR1)
NR_119373.1:n.102-843C>T (PCAT2)