Canonical Allele Identifier: CA1118964519
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1813766134

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091427A>G , CM000670.2:g.127091427A>G GRCh38
NC_000008.10:g.128103672A>G , CM000670.1:g.128103672A>G GRCh37
NC_000008.9:g.128172854A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11554A>G