Canonical Allele Identifier: CA223621040
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs925508701
MyVariant Identifiers: chr11:g.62758768T>C (hg19) chr11:g.62991296T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991296T>C , CM000673.2:g.62991296T>C GRCh38
NC_000011.9:g.62758768T>C , CM000673.1:g.62758768T>C GRCh37
NC_000011.8:g.62515344T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5436A>G
Search 100 bp 5'
Search 100 bp 3'