ClinGen Allele Registry
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Canonical Allele Identifier:
CA525390623
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.113761104A>C
GRCh37
chr1:g.114303726A>C
Linked Data - Sequence & Population
gnomAD v2:
1:114303726 A / C
Linked Data - NCBI & NCI
dbSNP:
1286451655
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.113761104A>C , CM000663.2:g.113761104A>C
GRCh38
NC_000001.10:g.114303726A>C , CM000663.1:g.114303726A>C
GRCh37
NC_000001.9:g.114105249A>C
NCBI36
Search 100 bp 5'
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