ClinGen Allele Registry
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Canonical Allele Identifier:
CA1978008821
Gene: SLC22A8
HGNC
NCBI
Linked Data
dbSNP Id:
rs2086346959
gnomAD v4:
11-62991265-A-G
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.62991265A>G , CM000673.2:g.62991265A>G
GRCh38
NC_000011.9:g.62758737A>G , CM000673.1:g.62758737A>G
GRCh37
NC_000011.8:g.62515313A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000539841.1:n.5467T>C
Search 100 bp 5'
Search 100 bp 3'