Canonical Allele Identifier: CA1118964646
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1034404120

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127092183T>C , CM000670.2:g.127092183T>C GRCh38
NC_000008.10:g.128104428T>C , CM000670.1:g.128104428T>C GRCh37
NC_000008.9:g.128173610T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12310T>C