Canonical Allele Identifier: CA727889901
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1269134066

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30219747C>T , CM000679.2:g.30219747C>T GRCh38
NC_000017.10:g.28546765C>T , CM000679.1:g.28546765C>T GRCh37
NC_000017.9:g.25570891C>T NCBI36
NG_011747.2:g.21190G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.344-816G>A MANE Select ENSP00000498537.1:n.344-816G>A
ENST00000261707.7:c.344-816G>A ENSP00000261707.3:n.344-816G>A
ENST00000394821.2:c.344-816G>A ENSP00000378298.2:n.344-816G>A
ENST00000401766.6:c.344-816G>A ENSP00000385822.2:n.344-816G>A
NM_001045.5:c.344-816G>A NP_001036.1:n.344-816G>A
NM_001045.6:c.344-816G>A MANE Select NP_001036.1:n.344-816G>A