Canonical Allele Identifier: CA1118986200
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813581336
gnomAD v3: 8-127080061-CA-C
gnomAD v4: 8-127080061-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080062del , CM000670.2:g.127080062del GRCh38
NC_000008.10:g.128092307del , CM000670.1:g.128092307del GRCh37
NC_000008.9:g.128161489del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.189del (PRNCR1)
NR_119373.1:n.102-929del (PCAT2)
Search 100 bp 5'
Search 100 bp 3'