ClinGen Allele Registry
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Canonical Allele Identifier:
CA14829496
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.46113425C>A
GRCh37
chr20:g.44742064C>A
Linked Data - Sequence & Population
gnomAD v2:
20:44742064 C / A
gnomAD v3:
20:46113425 C / A
gnomAD v4:
chr20-46113425-C-A
Joint Max Group AF
0.93154663 (AFR)
Genomes Max Group AF
0.93154663 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1569723
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.46113425C>A , CM000682.2:g.46113425C>A
GRCh38
NC_000020.10:g.44742064C>A , CM000682.1:g.44742064C>A
GRCh37
NC_000020.9:g.44175471C>A
NCBI36
NG_007279.1:g.159C>A , LRG_40:g.159C>A
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