Canonical Allele Identifier: CA1818178530
Gene: PRNCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091784T= , CM000670.2:g.127091784T= GRCh38
NC_000008.10:g.128104029T= , CM000670.1:g.128104029T= GRCh37
NC_000008.9:g.128173211T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.11911T=