Canonical Allele Identifier: CA1118964593
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1813771196

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091827C>T , CM000670.2:g.127091827C>T GRCh38
NC_000008.10:g.128104072C>T , CM000670.1:g.128104072C>T GRCh37
NC_000008.9:g.128173254C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11954C>T