Canonical Allele Identifier: CA1118986285

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1813584781
• gnomAD v3: 8-127080238-A-G
• gnomAD v4: 8-127080238-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080238A>G , CM000670.2:g.127080238A>G	GRCh38
NC_000008.10:g.128092483A>G , CM000670.1:g.128092483A>G	GRCh37
NC_000008.9:g.128161665A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.365A>G (PRNCR1)
NR_119373.1:n.102-1105T>C (PCAT2)