Canonical Allele Identifier: CA289284295
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs761484502
MyVariant Identifiers: chr17:g.28551561C>G (hg19) chr17:g.30224543C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224543C>G , CM000679.2:g.30224543C>G GRCh38
NC_000017.10:g.28551561C>G , CM000679.1:g.28551561C>G GRCh37
NC_000017.9:g.25575687C>G NCBI36
NG_011747.2:g.16394G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.-220-1628G>C MANE Select ENSP00000498537.1:n.-220-1628G>C
ENST00000261707.7:c.-220-1628G>C ENSP00000261707.3:n.-220-1628G>C
ENST00000394821.2:c.-220-1628G>C ENSP00000378298.2:n.-220-1628G>C
ENST00000401766.6:c.-123-2462G>C ENSP00000385822.2:n.-123-2462G>C
NM_001045.5:c.-220-1628G>C NP_001036.1:n.-220-1628G>C
NM_001045.6:c.-220-1628G>C MANE Select NP_001036.1:n.-220-1628G>C
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