ClinGen Allele Registry
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Canonical Allele Identifier:
CA97393472
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.54368658C>G
GRCh37
chr4:g.55234825C>G
Linked Data - Sequence & Population
gnomAD v2:
4:55234825 C / G
gnomAD v3:
4:54368658 C / G
gnomAD v4:
chr4-54368658-C-G
Joint Max Group AF
0.18898881 (NFE)
Genomes Max Group AF
0.18898881 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17690232
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.54368658C>G , CM000666.2:g.54368658C>G
GRCh38
NC_000004.11:g.55234825C>G , CM000666.1:g.55234825C>G
GRCh37
NC_000004.10:g.54929582C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'