Canonical Allele Identifier: CA1818225141

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1813582316
• gnomAD v4: 8-127080108-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080108T>A , CM000670.2:g.127080108T>A	GRCh38
NC_000008.10:g.128092353T>A , CM000670.1:g.128092353T>A	GRCh37
NC_000008.9:g.128161535T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.235T>A (PRNCR1)
NR_119373.1:n.102-975A>T (PCAT2)