ClinGen Allele Registry
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Canonical Allele Identifier:
CA100846915
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.87854091T>C
GRCh37
chr4:g.88775243T>C
Linked Data - Sequence & Population
gnomAD v2:
4:88775243 T / C
gnomAD v3:
4:87854091 T / C
gnomAD v4:
chr4-87854091-T-C
Joint Max Group AF
0.7099118 (AMR)
Genomes Max Group AF
0.7099118 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1471403
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.87854091T>C , CM000666.2:g.87854091T>C
GRCh38
NC_000004.11:g.88775243T>C , CM000666.1:g.88775243T>C
GRCh37
NC_000004.10:g.88994267T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'