Canonical Allele Identifier: CA847146989
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs757704533
gnomAD v4: 8-127092177-G-T
MyVariant Identifiers: chr8:g.128104422G>T (hg19) chr8:g.127092177G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127092177G>T , CM000670.2:g.127092177G>T GRCh38
NC_000008.10:g.128104422G>T , CM000670.1:g.128104422G>T GRCh37
NC_000008.9:g.128173604G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12304G>T
Search 100 bp 5'
Search 100 bp 3'