ClinGen Allele Registry
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Canonical Allele Identifier:
CA11496908
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.27723132A>G
GRCh37
chr3:g.27764623A>G
Linked Data - Sequence & Population
gnomAD v2:
3:27764623 A / G
gnomAD v3:
3:27723132 A / G
gnomAD v4:
chr3-27723132-A-G
Joint Max Group AF
0.82028735 (AFR)
Genomes Max Group AF
0.82028735 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3806624
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.27723132A>G , CM000665.2:g.27723132A>G
GRCh38
NC_000003.11:g.27764623A>G , CM000665.1:g.27764623A>G
GRCh37
NC_000003.10:g.27739627A>G
NCBI36
NG_042182.1:g.4584T>C
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