ClinGen Allele Registry
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Canonical Allele Identifier:
CA11697656
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.110778170T>C
GRCh37
chr4:g.111699326T>C
Linked Data - Sequence & Population
gnomAD v2:
4:111699326 T / C
gnomAD v3:
4:110778170 T / C
gnomAD v4:
chr4-110778170-T-C
Joint Max Group AF
0.48543178 (EAS)
Genomes Max Group AF
0.48543178 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12646447
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.110778170T>C , CM000666.2:g.110778170T>C
GRCh38
NC_000004.11:g.111699326T>C , CM000666.1:g.111699326T>C
GRCh37
NC_000004.10:g.111918775T>C
NCBI36
Search 100 bp 5'
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