Canonical Allele Identifier: CA1118964581
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1813769978

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091738G>A , CM000670.2:g.127091738G>A GRCh38
NC_000008.10:g.128103983G>A , CM000670.1:g.128103983G>A GRCh37
NC_000008.9:g.128173165G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.11865G>A