Canonical Allele Identifier: CA847139019
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1358785522
gnomAD v3: 8-127080298-C-T
gnomAD v4: 8-127080298-C-T
MyVariant Identifiers: chr8:g.128092543C>T (hg19) chr8:g.127080298C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080298C>T , CM000670.2:g.127080298C>T GRCh38
NC_000008.10:g.128092543C>T , CM000670.1:g.128092543C>T GRCh37
NC_000008.9:g.128161725C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.425C>T (PRNCR1)
NR_119373.1:n.102-1165G>A (PCAT2)
Search 100 bp 5'
Search 100 bp 3'