Canonical Allele Identifier: CA185700229
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs746103601

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091651T>G , CM000670.2:g.127091651T>G GRCh38
NC_000008.10:g.128103896T>G , CM000670.1:g.128103896T>G GRCh37
NC_000008.9:g.128173078T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11778T>G