Canonical Allele Identifier: CA398960614
Gene: SLC6A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.28548663A>T (hg19) chr17:g.30221645A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221645A>T , CM000679.2:g.30221645A>T GRCh38
NC_000017.10:g.28548663A>T , CM000679.1:g.28548663A>T GRCh37
NC_000017.9:g.25572789A>T NCBI36
NG_011747.2:g.19292T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.314T>A MANE Select ENSP00000498537.1:p.Phe105Tyr
ENST00000261707.7:c.314T>A ENSP00000261707.3:p.Phe105Tyr
ENST00000394821.2:c.314T>A ENSP00000378298.2:p.Phe105Tyr
ENST00000401766.6:c.314T>A ENSP00000385822.2:p.Phe105Tyr
NM_001045.5:c.314T>A NP_001036.1:p.Phe105Tyr
NM_001045.6:c.314T>A MANE Select NP_001036.1:p.Phe105Tyr
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