ClinGen Allele Registry
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Canonical Allele Identifier:
CA265019881
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.84131041G>C
GRCh37
chr14:g.84597385G>C
Linked Data - Sequence & Population
gnomAD v2:
14:84597385 G / C
gnomAD v3:
14:84131041 G / C
gnomAD v4:
chr14-84131041-G-C
Joint Max Group AF
0.0838569 (NFE)
Genomes Max Group AF
0.0838569 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7152554
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.84131041G>C , CM000676.2:g.84131041G>C
GRCh38
NC_000014.8:g.84597385G>C , CM000676.1:g.84597385G>C
GRCh37
NC_000014.7:g.83667138G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'