Canonical Allele Identifier: CA2255105309
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906382285
gnomAD v4: 17-30211431-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30211431C>G , CM000679.2:g.30211431C>G GRCh38
NC_000017.10:g.28538449C>G , CM000679.1:g.28538449C>G GRCh37
NC_000017.9:g.25562575C>G NCBI36
NG_011747.2:g.29506G>C

Transcript Alleles

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