Canonical Allele Identifier: CA1818224957

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1586763186

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127079879T>G , CM000670.2:g.127079879T>G	GRCh38
NC_000008.10:g.128092124T>G , CM000670.1:g.128092124T>G	GRCh37
NC_000008.9:g.128161306T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.6T>G (PRNCR1)
NR_119373.1:n.102-746A>C (PCAT2)