Canonical Allele Identifier: CA2688533354
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080237del , CM000670.2:g.127080237del GRCh38
NC_000008.10:g.128092482del , CM000670.1:g.128092482del GRCh37
NC_000008.9:g.128161664del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.364del (PRNCR1)
NR_119373.1:n.102-1104del (PCAT2)