ClinGen Allele Registry
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Canonical Allele Identifier:
CA13468916
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.102844317T>C
GRCh37
chr11:g.102715048T>C
Linked Data - Sequence & Population
gnomAD v2:
11:102715048 T / C
gnomAD v3:
11:102844317 T / C
gnomAD v4:
chr11-102844317-T-C
Joint Max Group AF
0.39120079 (SAS)
Genomes Max Group AF
0.39120079 (SAS)
Linked Data - NCBI & NCI
dbSNP:
522616
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.102844317T>C , CM000673.2:g.102844317T>C
GRCh38
NC_000011.9:g.102715048T>C , CM000673.1:g.102715048T>C
GRCh37
NC_000011.8:g.102220258T>C
NCBI36
NG_012100.1:g.4295A>G
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