Canonical Allele Identifier: CA15551158

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1016343
• gnomAD v2: 8-128093297-C-T
• gnomAD v3: 8-127081052-C-T
• gnomAD v4: 8-127081052-C-T
• MyVariant Identifiers: chr8:g.128093297C>T (hg19) ; chr8:g.127081052C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127081052C>T , CM000670.2:g.127081052C>T	GRCh38
NC_000008.10:g.128093297C>T , CM000670.1:g.128093297C>T	GRCh37
NC_000008.9:g.128162479C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.1179C>T (PRNCR1)
NR_119373.1:n.101+1069G>A (PCAT2)