Canonical Allele Identifier: CA223621091
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs113211994
gnomAD v2: 11-62758877-T-C
gnomAD v3: 11-62991405-T-C
gnomAD v4: 11-62991405-T-C
MyVariant Identifiers: chr11:g.62758877T>C (hg19) chr11:g.62991405T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5327A>G
Search 100 bp 5'
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