Canonical Allele Identifier: CA289280271
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs935504919
gnomAD v2: 17-28546810-G-C
gnomAD v3: 17-30219792-G-C
gnomAD v4: 17-30219792-G-C
MyVariant Identifiers: chr17:g.28546810G>C (hg19) chr17:g.30219792G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30219792G>C , CM000679.2:g.30219792G>C GRCh38
NC_000017.10:g.28546810G>C , CM000679.1:g.28546810G>C GRCh37
NC_000017.9:g.25570936G>C NCBI36
NG_011747.2:g.21145C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.344-861C>G MANE Select ENSP00000498537.1:n.344-861C>G
ENST00000261707.7:c.344-861C>G ENSP00000261707.3:n.344-861C>G
ENST00000394821.2:c.344-861C>G ENSP00000378298.2:n.344-861C>G
ENST00000401766.6:c.344-861C>G ENSP00000385822.2:n.344-861C>G
NM_001045.5:c.344-861C>G NP_001036.1:n.344-861C>G
NM_001045.6:c.344-861C>G MANE Select NP_001036.1:n.344-861C>G
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