Canonical Allele Identifier: CA185700263
Gene: PRNCR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 979039
ClinVar RCV Id: RCV001257962
dbSNP Id: rs183373024
gnomAD v2: 8-128104117-A-G
gnomAD v3: 8-127091872-A-G
gnomAD v4: 8-127091872-A-G
MyVariant Identifiers: chr8:g.128104117A>G (hg19) chr8:g.127091872A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091872A>G , CM000670.2:g.127091872A>G GRCh38
NC_000008.10:g.128104117A>G , CM000670.1:g.128104117A>G GRCh37
NC_000008.9:g.128173299A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.11999A>G
Search 100 bp 5'
Search 100 bp 3'