ClinGen Allele Registry
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Canonical Allele Identifier:
CA185700257
Gene: PRNCR1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1014791142
gnomAD v3:
8-127091828-T-G
gnomAD v4:
8-127091828-T-G
MyVariant Identifiers:
chr8:g.128104073T>G (hg19)
chr8:g.127091828T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127091828T>G , CM000670.2:g.127091828T>G
GRCh38
NC_000008.10:g.128104073T>G , CM000670.1:g.128104073T>G
GRCh37
NC_000008.9:g.128173255T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109833.1:n.11955T>G
Search 100 bp 5'
Search 100 bp 3'