Canonical Allele Identifier: CA2614031312
Gene: SLC22A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991261G>T , CM000673.2:g.62991261G>T GRCh38
NC_000011.9:g.62758733G>T , CM000673.1:g.62758733G>T GRCh37
NC_000011.8:g.62515309G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5471C>A