Canonical Allele Identifier: CA2255095361
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs536833142

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224506C>A , CM000679.2:g.30224506C>A GRCh38
NC_000017.10:g.28551524C>A , CM000679.1:g.28551524C>A GRCh37
NC_000017.9:g.25575650C>A NCBI36
NG_011747.2:g.16431G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-1591G>T MANE Select ENSP00000498537.1:n.-220-1591G>T
ENST00000261707.7:c.-220-1591G>T ENSP00000261707.3:n.-220-1591G>T
ENST00000394821.2:c.-220-1591G>T ENSP00000378298.2:n.-220-1591G>T
ENST00000401766.6:c.-123-2425G>T ENSP00000385822.2:n.-123-2425G>T
NM_001045.5:c.-220-1591G>T NP_001036.1:n.-220-1591G>T
NM_001045.6:c.-220-1591G>T MANE Select NP_001036.1:n.-220-1591G>T