ClinGen Allele Registry
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Canonical Allele Identifier:
CA11728806
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.87975645T>G
GRCh37
chr4:g.88896797T>G
Linked Data - Sequence & Population
gnomAD v2:
4:88896797 T / G
gnomAD v3:
4:87975645 T / G
gnomAD v4:
chr4-87975645-T-G
Joint Max Group AF
0.23156993 (NFE)
Genomes Max Group AF
0.23212591 (NFE)
Exomes Max Group AF
0.21299538 (NFE)
Linked Data - NCBI & NCI
dbSNP:
28357094
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.87975645T>G , CM000666.2:g.87975645T>G
GRCh38
NC_000004.11:g.88896797T>G , CM000666.1:g.88896797T>G
GRCh37
NC_000004.10:g.89115821T>G
NCBI36
NG_030362.1:g.4996T>G
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