Canonical Allele Identifier: CA185698789

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs541662586
• gnomAD v3: 8-127080151-A-G
• gnomAD v4: 8-127080151-A-G
• MyVariant Identifiers: chr8:g.128092396A>G (hg19) ; chr8:g.127080151A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080151A>G , CM000670.2:g.127080151A>G	GRCh38
NC_000008.10:g.128092396A>G , CM000670.1:g.128092396A>G	GRCh37
NC_000008.9:g.128161578A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.278A>G (PRNCR1)
NR_119373.1:n.102-1018T>C (PCAT2)