Canonical Allele Identifier: CA2614031323
Gene: SLC22A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991283A>G , CM000673.2:g.62991283A>G GRCh38
NC_000011.9:g.62758755A>G , CM000673.1:g.62758755A>G GRCh37
NC_000011.8:g.62515331A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5449T>C