Canonical Allele Identifier: CA585058139

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1434074147
• gnomAD v2: 8-128104374-C-T
• gnomAD v3: 8-127092129-C-T
• gnomAD v4: 8-127092129-C-T
• MyVariant Identifiers: chr8:g.128104374C>T (hg19) ; chr8:g.127092129C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127092129C>T , CM000670.2:g.127092129C>T	GRCh38
NC_000008.10:g.128104374C>T , CM000670.1:g.128104374C>T	GRCh37
NC_000008.9:g.128173556C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12256C>T