Canonical Allele Identifier: CA185698775

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1023068585
• gnomAD v2: 8-128092180-G-T
• gnomAD v3: 8-127079935-G-T
• gnomAD v4: 8-127079935-G-T
• MyVariant Identifiers: chr8:g.128092180G>T (hg19) ; chr8:g.127079935G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127079935G>T , CM000670.2:g.127079935G>T	GRCh38
NC_000008.10:g.128092180G>T , CM000670.1:g.128092180G>T	GRCh37
NC_000008.9:g.128161362G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.62G>T (PRNCR1)
NR_119373.1:n.102-802C>A (PCAT2)