ClinGen Allele Registry
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Canonical Allele Identifier:
CA99933054
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.73739815T>C
GRCh37
chr4:g.74605532T>C
Linked Data - Sequence & Population
gnomAD v2:
4:74605532 T / C
gnomAD v3:
4:73739815 T / C
gnomAD v4:
chr4-73739815-T-C
Joint Max Group AF
0.07992568 (AFR)
Genomes Max Group AF
0.07992568 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2227532
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.73739815T>C , CM000666.2:g.73739815T>C
GRCh38
NC_000004.11:g.74605532T>C , CM000666.1:g.74605532T>C
GRCh37
NC_000004.10:g.74824396T>C
NCBI36
NG_029889.1:g.4310T>C
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