Canonical Allele Identifier: CA289284287
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs920741467

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224520G>T , CM000679.2:g.30224520G>T GRCh38
NC_000017.10:g.28551538G>T , CM000679.1:g.28551538G>T GRCh37
NC_000017.9:g.25575664G>T NCBI36
NG_011747.2:g.16417C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.-220-1605C>A MANE Select ENSP00000498537.1:n.-220-1605C>A
ENST00000261707.7:c.-220-1605C>A ENSP00000261707.3:n.-220-1605C>A
ENST00000394821.2:c.-220-1605C>A ENSP00000378298.2:n.-220-1605C>A
ENST00000401766.6:c.-123-2439C>A ENSP00000385822.2:n.-123-2439C>A
NM_001045.5:c.-220-1605C>A NP_001036.1:n.-220-1605C>A
NM_001045.6:c.-220-1605C>A MANE Select NP_001036.1:n.-220-1605C>A