Canonical Allele Identifier: CA185698773

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs903284415
• gnomAD v3: 8-127079896-T-C
• gnomAD v4: 8-127079896-T-C
• MyVariant Identifiers: chr8:g.128092141T>C (hg19) ; chr8:g.127079896T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127079896T>C , CM000670.2:g.127079896T>C	GRCh38
NC_000008.10:g.128092141T>C , CM000670.1:g.128092141T>C	GRCh37
NC_000008.9:g.128161323T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.23T>C (PRNCR1)
NR_119373.1:n.102-763A>G (PCAT2)