Canonical Allele Identifier: CA2637002540
Gene: SLC6A4 HGNC NCBI

Linked Data

gnomAD v4: 17-30211535-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30211535A>C , CM000679.2:g.30211535A>C GRCh38
NC_000017.10:g.28538553A>C , CM000679.1:g.28538553A>C GRCh37
NC_000017.9:g.25562679A>C NCBI36
NG_011747.2:g.29402T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.1205-111T>G MANE Select ENSP00000498537.1:n.1205-111T>G
ENST00000261707.7:c.1205-111T>G ENSP00000261707.3:n.1205-111T>G
ENST00000394821.2:c.1205-111T>G ENSP00000378298.2:n.1205-111T>G
ENST00000401766.6:c.1205-111T>G ENSP00000385822.2:n.1205-111T>G
NM_001045.5:c.1205-111T>G NP_001036.1:n.1205-111T>G
NM_001045.6:c.1205-111T>G MANE Select NP_001036.1:n.1205-111T>G
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