Canonical Allele Identifier: CA223621044
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs958458483
gnomAD v2: 11-62758771-T-C
MyVariant Identifiers: chr11:g.62758771T>C (hg19) chr11:g.62991299T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991299T>C , CM000673.2:g.62991299T>C GRCh38
NC_000011.9:g.62758771T>C , CM000673.1:g.62758771T>C GRCh37
NC_000011.8:g.62515347T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5433A>G
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