Canonical Allele Identifier: CA14375991
Gene: SLC6A4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2020942

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30219896C>T , CM000679.2:g.30219896C>T GRCh38
NC_000017.9:g.25571040C>T NCBI36
NC_000017.10:g.28546914C>T , CM000679.1:g.28546914C>T GRCh37
NG_011747.2:g.21041G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261707.7:c.344-965G>A ENSP00000261707.3:p.=
ENST00000394821.2:c.344-965G>A ENSP00000378298.2:p.=
ENST00000401766.6:c.344-965G>A ENSP00000385822.2:p.=
NM_001045.5:c.344-965G>A VV NP_001036.1:p.=