ClinGen Allele Registry
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Canonical Allele Identifier:
CA847146653
Gene: PRNCR1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1194329267
gnomAD v3:
8-127091683-A-G
gnomAD v4:
8-127091683-A-G
MyVariant Identifiers:
chr8:g.128103928A>G (hg19)
chr8:g.127091683A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127091683A>G , CM000670.2:g.127091683A>G
GRCh38
NC_000008.10:g.128103928A>G , CM000670.1:g.128103928A>G
GRCh37
NC_000008.9:g.128173110A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109833.1:n.11810A>G
Search 100 bp 5'
Search 100 bp 3'