Canonical Allele Identifier: CA2567638070
Gene: SLC22A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991372G>C , CM000673.2:g.62991372G>C GRCh38
NC_000011.9:g.62758844G>C , CM000673.1:g.62758844G>C GRCh37
NC_000011.8:g.62515420G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5360C>G