Canonical Allele Identifier: CA679091770
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs1173418807
MyVariant Identifiers: chr11:g.62758563A>G (hg19) chr11:g.62991091A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991091A>G , CM000673.2:g.62991091A>G GRCh38
NC_000011.9:g.62758563A>G , CM000673.1:g.62758563A>G GRCh37
NC_000011.8:g.62515139A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5641T>C
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