ClinGen Allele Registry
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Canonical Allele Identifier:
CA2614031332
Gene: SLC22A8
HGNC
NCBI
Linked Data
gnomAD v4:
11-62991303-G-A
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.62991303G>A , CM000673.2:g.62991303G>A
GRCh38
NC_000011.9:g.62758775G>A , CM000673.1:g.62758775G>A
GRCh37
NC_000011.8:g.62515351G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000539841.1:n.5429C>T
Search 100 bp 5'
Search 100 bp 3'