Canonical Allele Identifier: CA13462152
Gene: SLC22A8 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.62991327C>G
GRCh37 chr11:g.62758799C>G
gnomAD v2:
11:62758799 C / G
gnomAD v3:
11:62991327 C / G
gnomAD v4:
chr11-62991327-C-G
Joint Max Group AF 0.52451694 (SAS)
Genomes Max Group AF 0.52451694 (SAS)
Exomes Max Group AF 0.17768 (EAS)
dbSNP:
10792367
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991327C>G , CM000673.2:g.62991327C>G GRCh38
NC_000011.9:g.62758799C>G , CM000673.1:g.62758799C>G GRCh37
NC_000011.8:g.62515375C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5405G>C
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