Canonical Allele Identifier: CA359083190
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756239605
MyVariant Identifiers: chr5:g.1414878A>T (hg19) chr5:g.1414763A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414763A>T , CM000667.2:g.1414763A>T GRCh38
NC_000005.9:g.1414878A>T , CM000667.1:g.1414878A>T GRCh37
NC_000005.8:g.1467878A>T NCBI36
NG_015885.1:g.35666T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1084T>A MANE Select ENSP00000270349.9:p.Phe362Ile
ENST00000270349.11:c.1084T>A ENSP00000270349.9:p.Phe362Ile
ENST00000511750.1:n.534T>A
NM_001044.4:c.1084T>A NP_001035.1:p.Phe362Ile
NM_001044.5:c.1084T>A MANE Select NP_001035.1:p.Phe362Ile
Search 100 bp 5'
Search 100 bp 3'