ClinGen Allele Registry
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Canonical Allele Identifier:
CA15319707
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.147479667C>A
GRCh37
chr4:g.148400819C>A
Linked Data - Sequence & Population
gnomAD v2:
4:148400819 C / A
gnomAD v3:
4:147479667 C / A
gnomAD v4:
chr4-147479667-C-A
Joint Max Group AF
0.39219635 (AFR)
Genomes Max Group AF
0.39219635 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6842241
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.147479667C>A , CM000666.2:g.147479667C>A
GRCh38
NC_000004.11:g.148400819C>A , CM000666.1:g.148400819C>A
GRCh37
NC_000004.10:g.148620269C>A
NCBI36
NG_013343.1:g.3751C>A
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