Canonical Allele Identifier: CA289291664
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs928298331

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30234722A>C , CM000679.2:g.30234722A>C GRCh38
NC_000017.10:g.28561740A>C , CM000679.1:g.28561740A>C GRCh37
NC_000017.9:g.25585866A>C NCBI36
NG_011747.2:g.6215T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-221+891T>G MANE Select ENSP00000498537.1:n.-221+891T>G
ENST00000261707.7:c.-221+891T>G ENSP00000261707.3:n.-221+891T>G
ENST00000394821.2:c.-221+891T>G ENSP00000378298.2:n.-221+891T>G
ENST00000401766.6:c.-124+891T>G ENSP00000385822.2:n.-124+891T>G
NM_001045.5:c.-221+891T>G NP_001036.1:n.-221+891T>G
NM_001045.6:c.-221+891T>G MANE Select NP_001036.1:n.-221+891T>G