ClinGen Allele Registry
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Canonical Allele Identifier:
CA15683815
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.57595144C>G
GRCh37
chr11:g.57362617C>G
Linked Data - Sequence & Population
gnomAD v2:
11:57362617 C / G
gnomAD v3:
11:57595144 C / G
gnomAD v4:
chr11-57595144-C-G
Joint Max Group AF
0.86865335 (AFR)
Genomes Max Group AF
0.86865335 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2509897
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.57595144C>G , CM000673.2:g.57595144C>G
GRCh38
NC_000011.9:g.57362617C>G , CM000673.1:g.57362617C>G
GRCh37
NC_000011.8:g.57119193C>G
NCBI36
NG_009625.1:g.2591C>G , LRG_105:g.2591C>G
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