Canonical Allele Identifier: CA185700282
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1032853396
gnomAD v3: 8-127092113-T-C
gnomAD v4: 8-127092113-T-C
MyVariant Identifiers: chr8:g.128104358T>C (hg19) chr8:g.127092113T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127092113T>C , CM000670.2:g.127092113T>C GRCh38
NC_000008.10:g.128104358T>C , CM000670.1:g.128104358T>C GRCh37
NC_000008.9:g.128173540T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12240T>C
Search 100 bp 5'
Search 100 bp 3'