Canonical Allele Identifier: CA1818225216
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080198_127080199delinsCT , CM000670.2:g.127080198_127080199delinsCT GRCh38
NC_000008.10:g.128092443_128092444delinsCT , CM000670.1:g.128092443_128092444delinsCT GRCh37
NC_000008.9:g.128161625_128161626delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.325_326delinsCT (PRNCR1)
NR_119373.1:n.102-1066_102-1065delinsAG (PCAT2)