Canonical Allele Identifier: CA2255095374
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906872648

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224533C>T , CM000679.2:g.30224533C>T GRCh38
NC_000017.10:g.28551551C>T , CM000679.1:g.28551551C>T GRCh37
NC_000017.9:g.25575677C>T NCBI36
NG_011747.2:g.16404G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.-220-1618G>A MANE Select ENSP00000498537.1:n.-220-1618G>A
ENST00000261707.7:c.-220-1618G>A ENSP00000261707.3:n.-220-1618G>A
ENST00000394821.2:c.-220-1618G>A ENSP00000378298.2:n.-220-1618G>A
ENST00000401766.6:c.-123-2452G>A ENSP00000385822.2:n.-123-2452G>A
NM_001045.5:c.-220-1618G>A NP_001036.1:n.-220-1618G>A
NM_001045.6:c.-220-1618G>A MANE Select NP_001036.1:n.-220-1618G>A