Canonical Allele Identifier: CA2614031333
Gene: SLC22A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991306A>G , CM000673.2:g.62991306A>G GRCh38
NC_000011.9:g.62758778A>G , CM000673.1:g.62758778A>G GRCh37
NC_000011.8:g.62515354A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5426T>C