Canonical Allele Identifier: CA2688533251
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079885del , CM000670.2:g.127079885del GRCh38
NC_000008.10:g.128092130del , CM000670.1:g.128092130del GRCh37
NC_000008.9:g.128161312del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12del (PRNCR1)
NR_119373.1:n.102-752del (PCAT2)