ClinGen Allele Registry
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Canonical Allele Identifier:
CA786412308
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122825787C>A
GRCh37
chr4:g.123746942C>A
Linked Data - Sequence & Population
gnomAD v3:
4:122825787 C / A
gnomAD v4:
chr4-122825787-C-A
Linked Data - NCBI & NCI
dbSNP:
308395
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122825787C>A , CM000666.2:g.122825787C>A
GRCh38
NC_000004.11:g.123746942C>A , CM000666.1:g.123746942C>A
GRCh37
NC_000004.10:g.123966392C>A
NCBI36
NG_029067.1:g.4080C>A
NG_029067.2:g.4080C>A
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