Canonical Allele Identifier: CA10648969
Gene: SLC6A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 322521
ClinVar RCV Id: RCV000308551
dbSNP Id: rs1042173

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30197993A>C , CM000679.2:g.30197993A>C GRCh38
NC_000017.10:g.28525011A>C , CM000679.1:g.28525011A>C GRCh37
NC_000017.9:g.25549137A>C NCBI36
NG_011747.2:g.42944T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.*463T>G MANE Select ENSP00000498537.1:p.=
ENST00000261707.7:c.*463T>G ENSP00000261707.3:p.=
ENST00000401766.6:c.*463T>G ENSP00000385822.2:p.=
ENST00000579221.5:n.997T>G
NM_001045.5:c.*463T>G NP_001036.1:p.=
NM_001045.6:c.*463T>G MANE Select NP_001036.1:p.=