ClinGen Allele Registry
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Canonical Allele Identifier:
CA1118964574
Gene: PRNCR1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1813769688
gnomAD v3:
8-127091725-A-C
gnomAD v4:
8-127091725-A-C
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127091725A>C , CM000670.2:g.127091725A>C
GRCh38
NC_000008.10:g.128103970A>C , CM000670.1:g.128103970A>C
GRCh37
NC_000008.9:g.128173152A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109833.1:n.11852A>C
Search 100 bp 5'
Search 100 bp 3'