ClinGen Allele Registry
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Canonical Allele Identifier:
CA885736833
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.113761201C>G
GRCh37
chr1:g.114303823C>G
Linked Data - Sequence & Population
gnomAD v3:
1:113761201 C / G
gnomAD v4:
chr1-113761201-C-G
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1445800107
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.113761201C>G , CM000663.2:g.113761201C>G
GRCh38
NC_000001.10:g.114303823C>G , CM000663.1:g.114303823C>G
GRCh37
NC_000001.9:g.114105346C>G
NCBI36
Search 100 bp 5'
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