Canonical Allele Identifier: CA847146952
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1376018289
gnomAD v3: 8-127092126-GC-G
gnomAD v4: 8-127092126-GC-G
MyVariant Identifiers: chr8:g.128104372del (hg19) chr8:g.127092127del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127092129del , CM000670.2:g.127092129del GRCh38
NC_000008.10:g.128104374del , CM000670.1:g.128104374del GRCh37
NC_000008.9:g.128173556del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12256del
Search 100 bp 5'
Search 100 bp 3'