ClinGen Allele Registry
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Canonical Allele Identifier:
CA601776863
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.113407981A>G
GRCh37
chr11:g.113278703A>G
Linked Data - Sequence & Population
gnomAD v2:
11:113278703 A / G
Linked Data - NCBI & NCI
dbSNP:
1265378096
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.113407981A>G , CM000673.2:g.113407981A>G
GRCh38
NC_000011.9:g.113278703A>G , CM000673.1:g.113278703A>G
GRCh37
NC_000011.8:g.112783913A>G
NCBI36
NG_008841.1:g.72299T>C
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