Canonical Allele Identifier: CA16537932
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs2020936

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30223796G>A , CM000679.2:g.30223796G>A GRCh38
NC_000017.10:g.28550814G>A , CM000679.1:g.28550814G>A GRCh37
NC_000017.9:g.25574940G>A NCBI36
NG_011747.2:g.17141C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.-220-881C>T MANE Select ENSP00000498537.1:n.-220-881C>T
ENST00000261707.7:c.-220-881C>T ENSP00000261707.3:n.-220-881C>T
ENST00000394821.2:c.-220-881C>T ENSP00000378298.2:n.-220-881C>T
ENST00000401766.6:c.-123-1715C>T ENSP00000385822.2:n.-123-1715C>T
NM_001045.5:c.-220-881C>T NP_001036.1:n.-220-881C>T
NM_001045.6:c.-220-881C>T MANE Select NP_001036.1:n.-220-881C>T