Canonical Allele Identifier: CA1118964634

Gene: PRNCR1

Linked Data

• dbSNP Id: rs562452295
• gnomAD v3: 8-127092125-C-A
• gnomAD v4: 8-127092125-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127092125C>A , CM000670.2:g.127092125C>A	GRCh38
NC_000008.10:g.128104370C>A , CM000670.1:g.128104370C>A	GRCh37
NC_000008.9:g.128173552C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12252C>A