Canonical Allele Identifier: CA14462691
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs16965628

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30228407G>C , CM000679.2:g.30228407G>C GRCh38
NC_000017.10:g.28555425G>C , CM000679.1:g.28555425G>C GRCh37
NC_000017.9:g.25579551G>C NCBI36
NG_011747.2:g.12530C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.-220-5492C>G MANE Select ENSP00000498537.1:n.-220-5492C>G
ENST00000261707.7:c.-220-5492C>G ENSP00000261707.3:n.-220-5492C>G
ENST00000394821.2:c.-220-5492C>G ENSP00000378298.2:n.-220-5492C>G
ENST00000401766.6:c.-123-6326C>G ENSP00000385822.2:n.-123-6326C>G
NM_001045.5:c.-220-5492C>G NP_001036.1:n.-220-5492C>G
NM_001045.6:c.-220-5492C>G MANE Select NP_001036.1:n.-220-5492C>G