Canonical Allele Identifier: CA585055308
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1347937830
gnomAD v2: 8-128092145-TAC-T
gnomAD v3: 8-127079900-TAC-T
gnomAD v4: 8-127079900-TAC-T
MyVariant Identifiers: chr8:g.128092146_128092147del (hg19) chr8:g.127079901_127079902del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079902_127079903del , CM000670.2:g.127079902_127079903del GRCh38
NC_000008.10:g.128092147_128092148del , CM000670.1:g.128092147_128092148del GRCh37
NC_000008.9:g.128161329_128161330del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.29_30del (PRNCR1)
NR_119373.1:n.102-769_102-768del (PCAT2)
Search 100 bp 5'
Search 100 bp 3'