ClinGen Allele Registry
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Canonical Allele Identifier:
CA847146707
Gene: PRNCR1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1400748313
MyVariant Identifiers:
chr8:g.128103974A>T (hg19)
chr8:g.127091729A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127091729A>T , CM000670.2:g.127091729A>T
GRCh38
NC_000008.10:g.128103974A>T , CM000670.1:g.128103974A>T
GRCh37
NC_000008.9:g.128173156A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109833.1:n.11856A>T
Search 100 bp 5'
Search 100 bp 3'