Canonical Allele Identifier: CA1818178876
Gene: PRNCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127092172T= , CM000670.2:g.127092172T= GRCh38
NC_000008.10:g.128104417T= , CM000670.1:g.128104417T= GRCh37
NC_000008.9:g.128173599T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12299T=