ClinGen Allele Registry
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Canonical Allele Identifier:
CA124946901
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.111131801C>T
GRCh37
chr5:g.110467499C>T
Linked Data - Sequence & Population
gnomAD v2:
5:110467499 C / T
gnomAD v3:
5:111131801 C / T
gnomAD v4:
chr5-111131801-C-T
Joint Max Group AF
0.79006332 (SAS)
Genomes Max Group AF
0.79006332 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1438673
2126599622
2126599627
2126599638
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.111131801C>T , CM000667.2:g.111131801C>T
GRCh38
NC_000005.9:g.110467499C>T , CM000667.1:g.110467499C>T
GRCh37
NC_000005.8:g.110495398C>T
NCBI36
NG_008979.1:g.44630C>T
Search 100 bp 5'
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