ClinGen Allele Registry
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Canonical Allele Identifier:
CA13451939
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.128890715G>C
GRCh37
chr11:g.128760610G>C
Linked Data - Sequence & Population
gnomAD v2:
11:128760610 G / C
gnomAD v3:
11:128890715 G / C
gnomAD v4:
chr11-128890715-G-C
Joint Max Group AF
0.21052931 (NFE)
Genomes Max Group AF
0.21052931 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11221497
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.128890715G>C , CM000673.2:g.128890715G>C
GRCh38
NC_000011.9:g.128760610G>C , CM000673.1:g.128760610G>C
GRCh37
NC_000011.8:g.128265820G>C
NCBI36
NG_023406.2:g.4298G>C , LRG_333:g.4298G>C
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