Canonical Allele Identifier: CA2792377508
Gene: SLC22A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991319T>C , CM000673.2:g.62991319T>C GRCh38
NC_000011.9:g.62758791T>C , CM000673.1:g.62758791T>C GRCh37
NC_000011.8:g.62515367T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5413A>G