ClinGen Allele Registry
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Canonical Allele Identifier:
CA11725800
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.68672015T>G
GRCh37
chr4:g.69537733T>G
Linked Data - Sequence & Population
gnomAD v2:
4:69537733 T / G
gnomAD v3:
4:68672015 T / G
gnomAD v4:
chr4-68672015-T-G
Joint Max Group AF
0.60185296 (AFR)
Genomes Max Group AF
0.60185296 (AFR)
Linked Data - NCBI & NCI
dbSNP:
13112099
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.68672015T>G , CM000666.2:g.68672015T>G
GRCh38
NC_000004.11:g.69537733T>G , CM000666.1:g.69537733T>G
GRCh37
NC_000004.10:g.69220328T>G
NCBI36
NG_052676.1:g.3762A>C
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