Canonical Allele Identifier: CA1118964521
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1813766367
gnomAD v3: 8-127091441-C-T
gnomAD v4: 8-127091441-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091441C>T , CM000670.2:g.127091441C>T GRCh38
NC_000008.10:g.128103686C>T , CM000670.1:g.128103686C>T GRCh37
NC_000008.9:g.128172868C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11568C>T
Search 100 bp 5'
Search 100 bp 3'