Canonical Allele Identifier: CA398960572
Gene: SLC6A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.28548646G>T (hg19) chr17:g.30221628G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221628G>T , CM000679.2:g.30221628G>T GRCh38
NC_000017.10:g.28548646G>T , CM000679.1:g.28548646G>T GRCh37
NC_000017.9:g.25572772G>T NCBI36
NG_011747.2:g.19309C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.331C>A MANE Select ENSP00000498537.1:p.Gln111Lys
ENST00000261707.7:c.331C>A ENSP00000261707.3:p.Gln111Lys
ENST00000394821.2:c.331C>A ENSP00000378298.2:p.Gln111Lys
ENST00000401766.6:c.331C>A ENSP00000385822.2:p.Gln111Lys
NM_001045.5:c.331C>A NP_001036.1:p.Gln111Lys
NM_001045.6:c.331C>A MANE Select NP_001036.1:p.Gln111Lys
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