Canonical Allele Identifier: CA1118964574
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1813769688

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091725A>C , CM000670.2:g.127091725A>C GRCh38
NC_000008.10:g.128103970A>C , CM000670.1:g.128103970A>C GRCh37
NC_000008.9:g.128173152A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11852A>C