Canonical Allele Identifier: CA1118986282

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1813584740
• gnomAD v3: 8-127080237-T-C
• gnomAD v4: 8-127080237-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080237T>C , CM000670.2:g.127080237T>C	GRCh38
NC_000008.10:g.128092482T>C , CM000670.1:g.128092482T>C	GRCh37
NC_000008.9:g.128161664T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.364T>C (PRNCR1)
NR_119373.1:n.102-1104A>G (PCAT2)