Canonical Allele Identifier: CA1818225293

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1586763300
• gnomAD v4: 8-127080262-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080262G>A , CM000670.2:g.127080262G>A	GRCh38
NC_000008.10:g.128092507G>A , CM000670.1:g.128092507G>A	GRCh37
NC_000008.9:g.128161689G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.389G>A (PRNCR1)
NR_119373.1:n.102-1129C>T (PCAT2)