Canonical Allele Identifier: CA185698794
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs932628205
gnomAD v3: 8-127080201-G-A
gnomAD v4: 8-127080201-G-A
MyVariant Identifiers: chr8:g.128092446G>A (hg19) chr8:g.127080201G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080201G>A , CM000670.2:g.127080201G>A GRCh38
NC_000008.10:g.128092446G>A , CM000670.1:g.128092446G>A GRCh37
NC_000008.9:g.128161628G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.328G>A (PRNCR1)
NR_119373.1:n.102-1068C>T (PCAT2)
Search 100 bp 5'
Search 100 bp 3'