ClinGen Allele Registry
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Canonical Allele Identifier:
CA679145055
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.636784T>G
GRCh37
chr11:g.636784T>G
Linked Data - Sequence & Population
gnomAD v3:
11:636784 T / G
gnomAD v4:
chr11-636784-T-G
Linked Data - NCBI & NCI
ClinVar RCV:
RCV003313815
ClinVar Variation:
2135980
dbSNP:
1800955
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.636784T>G , CM000673.2:g.636784T>G
GRCh38
NC_000011.9:g.636784T>G , CM000673.1:g.636784T>G
GRCh37
NC_000011.8:g.626784T>G
NCBI36
NG_021241.1:g.4480T>G
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