Canonical Allele Identifier: CA1978008714
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs2086346316
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991116G>C , CM000673.2:g.62991116G>C GRCh38
NC_000011.9:g.62758588G>C , CM000673.1:g.62758588G>C GRCh37
NC_000011.8:g.62515164G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5616C>G
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