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Canonical Allele Identifier:
CA15547305
Gene: PRNCR1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.127091692T>C
GRCh37
chr8:g.128103937T>C
Linked Data - Sequence & Population
gnomAD v2:
8:128103937 T / C
gnomAD v3:
8:127091692 T / C
gnomAD v4:
chr8-127091692-T-C
Joint Max Group AF
0.66949084 (NFE)
Genomes Max Group AF
0.66949084 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1456315
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127091692T>C , CM000670.2:g.127091692T>C
GRCh38
NC_000008.10:g.128103937T>C , CM000670.1:g.128103937T>C
GRCh37
NC_000008.9:g.128173119T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109833.1:n.11819T>C
Search 100 bp 5'
Search 100 bp 3'