Canonical Allele Identifier: CA847146981

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1176200302
• gnomAD v3: 8-127092168-C-A
• gnomAD v4: 8-127092168-C-A
• MyVariant Identifiers: chr8:g.128104413C>A (hg19) ; chr8:g.127092168C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127092168C>A , CM000670.2:g.127092168C>A	GRCh38
NC_000008.10:g.128104413C>A , CM000670.1:g.128104413C>A	GRCh37
NC_000008.9:g.128173595C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12295C>A