Canonical Allele Identifier: CA982892261
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1905914418
gnomAD v3: 17-30197914-T-C
gnomAD v4: 17-30197914-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30197914T>C , CM000679.2:g.30197914T>C GRCh38
NC_000017.10:g.28524932T>C , CM000679.1:g.28524932T>C GRCh37
NC_000017.9:g.25549058T>C NCBI36
NG_011747.2:g.43023A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.*542A>G MANE Select ENSP00000498537.1:n.*542A>G
ENST00000261707.7:c.*542A>G ENSP00000261707.3:n.*542A>G
ENST00000401766.6:c.*542A>G ENSP00000385822.2:n.*542A>G
NM_001045.5:c.*542A>G NP_001036.1:n.*542A>G
NM_001045.6:c.*542A>G MANE Select NP_001036.1:n.*542A>G
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Search 100 bp 3'