Canonical Allele Identifier: CA359083834
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1416231A>C (hg19) chr5:g.1416116A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416116A>C , CM000667.2:g.1416116A>C GRCh38
NC_000005.9:g.1416231A>C , CM000667.1:g.1416231A>C GRCh37
NC_000005.8:g.1469231A>C NCBI36
NG_015885.1:g.34313T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1013T>G MANE Select ENSP00000270349.9:p.Phe338Cys
ENST00000270349.11:c.1013T>G ENSP00000270349.9:p.Phe338Cys
ENST00000511750.1:n.463T>G
NM_001044.4:c.1013T>G NP_001035.1:p.Phe338Cys
NM_001044.5:c.1013T>G MANE Select NP_001035.1:p.Phe338Cys
Search 100 bp 5'
Search 100 bp 3'