Canonical Allele Identifier: CA847138873

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1415027850
• MyVariant Identifiers: chr8:g.128092267A>C (hg19) ; chr8:g.127080022A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080022A>C , CM000670.2:g.127080022A>C	GRCh38
NC_000008.10:g.128092267A>C , CM000670.1:g.128092267A>C	GRCh37
NC_000008.9:g.128161449A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.149A>C (PRNCR1)
NR_119373.1:n.102-889T>G (PCAT2)