ClinGen Allele Registry
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Canonical Allele Identifier:
CA15704486
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.102876821G>C
GRCh37
chr11:g.102747551G>C
Linked Data - Sequence & Population
gnomAD v2:
11:102747551 G / C
gnomAD v3:
11:102876821 G / C
gnomAD v4:
chr11-102876821-G-C
Joint Max Group AF
0.31804206 (AFR)
Genomes Max Group AF
0.31804206 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1277718
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.102876821G>C , CM000673.2:g.102876821G>C
GRCh38
NC_000011.9:g.102747551G>C , CM000673.1:g.102747551G>C
GRCh37
NC_000011.8:g.102252761G>C
NCBI36
NG_032936.1:g.3214C>G
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