Canonical Allele Identifier: CA847138945

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1188598130
• gnomAD v4: 8-127080150-C-T
• MyVariant Identifiers: chr8:g.128092395C>T (hg19) ; chr8:g.127080150C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080150C>T , CM000670.2:g.127080150C>T	GRCh38
NC_000008.10:g.128092395C>T , CM000670.1:g.128092395C>T	GRCh37
NC_000008.9:g.128161577C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.277C>T (PRNCR1)
NR_119373.1:n.102-1017G>A (PCAT2)