Canonical Allele Identifier: CA1818178346
Gene: PRNCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091608A= , CM000670.2:g.127091608A= GRCh38
NC_000008.10:g.128103853A= , CM000670.1:g.128103853A= GRCh37
NC_000008.9:g.128173035A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.11735A=