ClinGen Allele Registry
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Canonical Allele Identifier:
CA800725955
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.99353050T>C
GRCh37
chr4:g.100274207T>C
Linked Data - Sequence & Population
gnomAD v3:
4:99353050 T / C
gnomAD v4:
chr4-99353050-T-C
Linked Data - NCBI & NCI
dbSNP:
1484225469
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99353050T>C , CM000666.2:g.99353050T>C
GRCh38
NC_000004.11:g.100274207T>C , CM000666.1:g.100274207T>C
GRCh37
NC_000004.10:g.100493230T>C
NCBI36
NG_011718.1:g.4711A>G
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