Canonical Allele Identifier: CA679091787
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs1344679849
gnomAD v3: 11-62991124-T-A
gnomAD v4: 11-62991124-T-A
MyVariant Identifiers: chr11:g.62758596T>A (hg19) chr11:g.62991124T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991124T>A , CM000673.2:g.62991124T>A GRCh38
NC_000011.9:g.62758596T>A , CM000673.1:g.62758596T>A GRCh37
NC_000011.8:g.62515172T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5608A>T
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