Canonical Allele Identifier: CA126861
Gene: SLC6A3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16763
ClinVar RCV Id: RCV000018249
dbSNP Id: rs267607068

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414744A>T , CM000667.2:g.1414744A>T GRCh38
NC_000005.8:g.1467859A>T NCBI36
NC_000005.9:g.1414859A>T , CM000667.1:g.1414859A>T GRCh37
NG_015885.1:g.35685T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.11:c.1103T>A ENSP00000270349.9:p.Leu368Gln
ENST00000511750.1:n.553T>A
NM_001044.4:c.1103T>A VV NP_001035.1:p.Leu368Gln