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Canonical Allele Identifier:
CA185700261
Gene: PRNCR1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1020118805
gnomAD v2:
8-128104104-C-T
gnomAD v3:
8-127091859-C-T
gnomAD v4:
8-127091859-C-T
MyVariant Identifiers:
chr8:g.128104104C>T (hg19)
chr8:g.127091859C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127091859C>T , CM000670.2:g.127091859C>T
GRCh38
NC_000008.10:g.128104104C>T , CM000670.1:g.128104104C>T
GRCh37
NC_000008.9:g.128173286C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109833.1:n.11986C>T
Search 100 bp 5'
Search 100 bp 3'