Canonical Allele Identifier: CA2255095355
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906871403

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224495G>C , CM000679.2:g.30224495G>C GRCh38
NC_000017.10:g.28551513G>C , CM000679.1:g.28551513G>C GRCh37
NC_000017.9:g.25575639G>C NCBI36
NG_011747.2:g.16442C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-1580C>G MANE Select ENSP00000498537.1:n.-220-1580C>G
ENST00000261707.7:c.-220-1580C>G ENSP00000261707.3:n.-220-1580C>G
ENST00000394821.2:c.-220-1580C>G ENSP00000378298.2:n.-220-1580C>G
ENST00000401766.6:c.-123-2414C>G ENSP00000385822.2:n.-123-2414C>G
NM_001045.5:c.-220-1580C>G NP_001036.1:n.-220-1580C>G
NM_001045.6:c.-220-1580C>G MANE Select NP_001036.1:n.-220-1580C>G