Canonical Allele Identifier: CA185698792
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs921282265
gnomAD v3: 8-127080198-CT-C
gnomAD v4: 8-127080198-CT-C
MyVariant Identifiers: chr8:g.128092444del (hg19) chr8:g.127080199del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080200del , CM000670.2:g.127080200del GRCh38
NC_000008.10:g.128092445del , CM000670.1:g.128092445del GRCh37
NC_000008.9:g.128161627del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.327del (PRNCR1)
NR_119373.1:n.102-1066del (PCAT2)
Search 100 bp 5'
Search 100 bp 3'