Canonical Allele Identifier: CA1978008920
Gene: SLC22A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991405T= , CM000673.2:g.62991405T= GRCh38
NC_000011.9:g.62758877T= , CM000673.1:g.62758877T= GRCh37
NC_000011.8:g.62515453T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5327A=