ClinGen Allele Registry
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Canonical Allele Identifier:
CA11559468
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.148697197T>G
GRCh37
chr3:g.148414984T>G
Linked Data - Sequence & Population
gnomAD v2:
3:148414984 T / G
gnomAD v3:
3:148697197 T / G
gnomAD v4:
chr3-148697197-T-G
Joint Max Group AF
0.25190633 (AFR)
Genomes Max Group AF
0.25190633 (AFR)
Linked Data - NCBI & NCI
dbSNP:
275652
2125149319
2125149321
2125149328
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.148697197T>G , CM000665.2:g.148697197T>G
GRCh38
NC_000003.11:g.148414984T>G , CM000665.1:g.148414984T>G
GRCh37
NC_000003.10:g.149897674T>G
NCBI36
NG_008468.1:g.4327T>G
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