ClinGen Allele Registry
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Canonical Allele Identifier:
CA311089305
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.4685463T>G
GRCh37
chr20:g.4666109T>G
Linked Data - Sequence & Population
gnomAD v2:
20:4666109 T / G
gnomAD v3:
20:4685463 T / G
gnomAD v4:
chr20-4685463-T-G
Joint Max Group AF
0.24219926 (AFR)
Genomes Max Group AF
0.24219926 (AFR)
Linked Data - NCBI & NCI
dbSNP:
57633656
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.4685463T>G , CM000682.2:g.4685463T>G
GRCh38
NC_000020.10:g.4666109T>G , CM000682.1:g.4666109T>G
GRCh37
NC_000020.9:g.4614109T>G
NCBI36
NG_009087.1:g.4313T>G
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