Canonical Allele Identifier: CA3186161
Gene: SLC6A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 538063
ClinVar RCV Id: RCV002235255
dbSNP Id: rs750843353
ExAC: 5:1414875 C / T
gnomAD v2: 5-1414875-C-T
gnomAD v3: 5-1414760-C-T
gnomAD v4: 5-1414760-C-T
MyVariant Identifiers: chr5:g.1414875C>T (hg19) chr5:g.1414760C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414760C>T , CM000667.2:g.1414760C>T GRCh38
NC_000005.9:g.1414875C>T , CM000667.1:g.1414875C>T GRCh37
NC_000005.8:g.1467875C>T NCBI36
NG_015885.1:g.35669G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1087G>A MANE Select ENSP00000270349.9:p.Val363Ile
ENST00000270349.11:c.1087G>A ENSP00000270349.9:p.Val363Ile
ENST00000511750.1:n.537G>A
NM_001044.4:c.1087G>A NP_001035.1:p.Val363Ile
NM_001044.5:c.1087G>A MANE Select NP_001035.1:p.Val363Ile
Search 100 bp 5'
Search 100 bp 3'