Canonical Allele Identifier: CA1818225130

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1813582186

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080102A>G , CM000670.2:g.127080102A>G	GRCh38
NC_000008.10:g.128092347A>G , CM000670.1:g.128092347A>G	GRCh37
NC_000008.9:g.128161529A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.229A>G (PRNCR1)
NR_119373.1:n.102-969T>C (PCAT2)