Canonical Allele Identifier: CA1818225245

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1813584649
• gnomAD v3: 8-127080227-C-T
• gnomAD v4: 8-127080227-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080227C>T , CM000670.2:g.127080227C>T	GRCh38
NC_000008.10:g.128092472C>T , CM000670.1:g.128092472C>T	GRCh37
NC_000008.9:g.128161654C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.354C>T (PRNCR1)
NR_119373.1:n.102-1094G>A (PCAT2)