Canonical Allele Identifier: CA915698851
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1563825854

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127092170T>A , CM000670.2:g.127092170T>A GRCh38
NC_000008.10:g.128104415T>A , CM000670.1:g.128104415T>A GRCh37
NC_000008.9:g.128173597T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12297T>A