Canonical Allele Identifier: CA2255095584
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906888431

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30225083T>C , CM000679.2:g.30225083T>C GRCh38
NC_000017.10:g.28552101T>C , CM000679.1:g.28552101T>C GRCh37
NC_000017.9:g.25576227T>C NCBI36
NG_011747.2:g.15854A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-2168A>G MANE Select ENSP00000498537.1:n.-220-2168A>G
ENST00000261707.7:c.-220-2168A>G ENSP00000261707.3:n.-220-2168A>G
ENST00000394821.2:c.-220-2168A>G ENSP00000378298.2:n.-220-2168A>G
ENST00000401766.6:c.-123-3002A>G ENSP00000385822.2:n.-123-3002A>G
NM_001045.5:c.-220-2168A>G NP_001036.1:n.-220-2168A>G
NM_001045.6:c.-220-2168A>G MANE Select NP_001036.1:n.-220-2168A>G