Canonical Allele Identifier: CA1118986275

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1813584515
• gnomAD v3: 8-127080220-A-G
• gnomAD v4: 8-127080220-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080220A>G , CM000670.2:g.127080220A>G	GRCh38
NC_000008.10:g.128092465A>G , CM000670.1:g.128092465A>G	GRCh37
NC_000008.9:g.128161647A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.347A>G (PRNCR1)
NR_119373.1:n.102-1087T>C (PCAT2)