Canonical Allele Identifier: CA1818178458
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1813769567

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091723A>C , CM000670.2:g.127091723A>C GRCh38
NC_000008.10:g.128103968A>C , CM000670.1:g.128103968A>C GRCh37
NC_000008.9:g.128173150A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.11850A>C