ClinGen Allele Registry
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Canonical Allele Identifier:
CA11559469
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.148697758A>G
GRCh37
chr3:g.148415545A>G
Linked Data - Sequence & Population
gnomAD v2:
3:148415545 A / G
gnomAD v3:
3:148697758 A / G
gnomAD v4:
chr3-148697758-A-G
Joint Max Group AF
0.25384924 (AFR)
Genomes Max Group AF
0.25384924 (AFR)
Exomes Max Group AF
0.08208867 (NFE)
Linked Data - NCBI & NCI
dbSNP:
275653
2125149382
2125149385
2125149389
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.148697758A>G , CM000665.2:g.148697758A>G
GRCh38
NC_000003.11:g.148415545A>G , CM000665.1:g.148415545A>G
GRCh37
NC_000003.10:g.149898235A>G
NCBI36
NG_008468.1:g.4888A>G
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