Canonical Allele Identifier: CA398960578
Gene: SLC6A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.28548648T>C (hg19) chr17:g.30221630T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221630T>C , CM000679.2:g.30221630T>C GRCh38
NC_000017.10:g.28548648T>C , CM000679.1:g.28548648T>C GRCh37
NC_000017.9:g.25572774T>C NCBI36
NG_011747.2:g.19307A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.329A>G MANE Select ENSP00000498537.1:p.Tyr110Cys
ENST00000261707.7:c.329A>G ENSP00000261707.3:p.Tyr110Cys
ENST00000394821.2:c.329A>G ENSP00000378298.2:p.Tyr110Cys
ENST00000401766.6:c.329A>G ENSP00000385822.2:p.Tyr110Cys
NM_001045.5:c.329A>G NP_001036.1:p.Tyr110Cys
NM_001045.6:c.329A>G MANE Select NP_001036.1:p.Tyr110Cys
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