Canonical Allele Identifier: CA847138793
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1196834359
MyVariant Identifiers: chr8:g.128092131C>T (hg19) chr8:g.127079886C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079886C>T , CM000670.2:g.127079886C>T GRCh38
NC_000008.10:g.128092131C>T , CM000670.1:g.128092131C>T GRCh37
NC_000008.9:g.128161313C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.13C>T (PRNCR1)
NR_119373.1:n.102-753G>A (PCAT2)
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