Canonical Allele Identifier: CA727893186
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1412569223
MyVariant Identifiers: chr17:g.28552132T>C (hg19) chr17:g.30225114T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30225114T>C , CM000679.2:g.30225114T>C GRCh38
NC_000017.10:g.28552132T>C , CM000679.1:g.28552132T>C GRCh37
NC_000017.9:g.25576258T>C NCBI36
NG_011747.2:g.15823A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-2199A>G MANE Select ENSP00000498537.1:n.-220-2199A>G
ENST00000261707.7:c.-220-2199A>G ENSP00000261707.3:n.-220-2199A>G
ENST00000394821.2:c.-220-2199A>G ENSP00000378298.2:n.-220-2199A>G
ENST00000401766.6:c.-123-3033A>G ENSP00000385822.2:n.-123-3033A>G
NM_001045.5:c.-220-2199A>G NP_001036.1:n.-220-2199A>G
NM_001045.6:c.-220-2199A>G MANE Select NP_001036.1:n.-220-2199A>G
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