Canonical Allele Identifier: CA652783023
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1335039611
gnomAD v3: 8-127091874-T-C
gnomAD v4: 8-127091874-T-C
COSMIC: COSN5674109
MyVariant Identifiers: chr8:g.128104119T>C (hg19) chr8:g.127091874T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091874T>C , CM000670.2:g.127091874T>C GRCh38
NC_000008.10:g.128104119T>C , CM000670.1:g.128104119T>C GRCh37
NC_000008.9:g.128173301T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12001T>C
Search 100 bp 5'
Search 100 bp 3'