Canonical Allele Identifier: CA847146756
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1471822663
gnomAD v3: 8-127091854-A-C
gnomAD v4: 8-127091854-A-C
MyVariant Identifiers: chr8:g.128104099A>C (hg19) chr8:g.127091854A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091854A>C , CM000670.2:g.127091854A>C GRCh38
NC_000008.10:g.128104099A>C , CM000670.1:g.128104099A>C GRCh37
NC_000008.9:g.128173281A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11981A>C
Search 100 bp 5'
Search 100 bp 3'