Canonical Allele Identifier: CA11025144
Gene:
COSMIC:
COSN6674233 (not active)
MyVariant.info:
GRCh38 chr2:g.112838252C>G
GRCh37 chr2:g.113595829C>G
gnomAD v2:
2:113595829 C / G
gnomAD v3:
2:112838252 C / G
gnomAD v4:
chr2-112838252-C-G
Joint Max Group AF 0.39102483 (AMR)
Genomes Max Group AF 0.39102483 (AMR)
ClinVar RCV:
RCV001078163
ClinVar Variation:
869139
dbSNP:
1143623
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112838252C>G , CM000664.2:g.112838252C>G GRCh38
NC_000002.11:g.113595829C>G , CM000664.1:g.113595829C>G GRCh37
NC_000002.10:g.113312300C>G NCBI36
NG_008851.1:g.3528G>C
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