Canonical Allele Identifier: CA289291678
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs916740867
gnomAD v3: 17-30234738-G-A
gnomAD v4: 17-30234738-G-A
MyVariant Identifiers: chr17:g.28561756G>A (hg19) chr17:g.30234738G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30234738G>A , CM000679.2:g.30234738G>A GRCh38
NC_000017.10:g.28561756G>A , CM000679.1:g.28561756G>A GRCh37
NC_000017.9:g.25585882G>A NCBI36
NG_011747.2:g.6199C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.-221+875C>T MANE Select ENSP00000498537.1:n.-221+875C>T
ENST00000261707.7:c.-221+875C>T ENSP00000261707.3:n.-221+875C>T
ENST00000394821.2:c.-221+875C>T ENSP00000378298.2:n.-221+875C>T
ENST00000401766.6:c.-124+875C>T ENSP00000385822.2:n.-124+875C>T
NM_001045.5:c.-221+875C>T NP_001036.1:n.-221+875C>T
NM_001045.6:c.-221+875C>T MANE Select NP_001036.1:n.-221+875C>T
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