Canonical Allele Identifier: CA1118964640
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1813776597

Genomic Alleles

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

Transcript Alleles

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