Canonical Allele Identifier: CA727893165
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1378641918
gnomAD v3: 17-30225077-G-A
gnomAD v4: 17-30225077-G-A
MyVariant Identifiers: chr17:g.28552095G>A (hg19) chr17:g.30225077G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30225077G>A , CM000679.2:g.30225077G>A GRCh38
NC_000017.10:g.28552095G>A , CM000679.1:g.28552095G>A GRCh37
NC_000017.9:g.25576221G>A NCBI36
NG_011747.2:g.15860C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-2162C>T MANE Select ENSP00000498537.1:n.-220-2162C>T
ENST00000261707.7:c.-220-2162C>T ENSP00000261707.3:n.-220-2162C>T
ENST00000394821.2:c.-220-2162C>T ENSP00000378298.2:n.-220-2162C>T
ENST00000401766.6:c.-123-2996C>T ENSP00000385822.2:n.-123-2996C>T
NM_001045.5:c.-220-2162C>T NP_001036.1:n.-220-2162C>T
NM_001045.6:c.-220-2162C>T MANE Select NP_001036.1:n.-220-2162C>T
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