ClinGen Allele Registry
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Canonical Allele Identifier:
CA257380410
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.20363635G>C
GRCh37
chr14:g.20831794G>C
Linked Data - Sequence & Population
gnomAD v2:
14:20831794 G / C
gnomAD v3:
14:20363635 G / C
gnomAD v4:
chr14-20363635-G-C
Joint Max Group AF
0.11032089 (SAS)
Genomes Max Group AF
0.11032089 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10143407
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.20363635G>C , CM000676.2:g.20363635G>C
GRCh38
NC_000014.8:g.20831794G>C , CM000676.1:g.20831794G>C
GRCh37
NC_000014.7:g.19901634G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'