Canonical Allele Identifier: CA223621086
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs1019513840
MyVariant Identifiers: chr11:g.62758868G>T (hg19) chr11:g.62991396G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991396G>T , CM000673.2:g.62991396G>T GRCh38
NC_000011.9:g.62758868G>T , CM000673.1:g.62758868G>T GRCh37
NC_000011.8:g.62515444G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5336C>A
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