Canonical Allele Identifier: CA289280241

Gene: SLC6A4

Linked Data

• dbSNP Id: rs969330746
• gnomAD v2: 17-28546755-T-C
• gnomAD v3: 17-30219737-T-C
• gnomAD v4: 17-30219737-T-C
• MyVariant Identifiers: chr17:g.28546755T>C (hg19) ; chr17:g.30219737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30219737T>C , CM000679.2:g.30219737T>C	GRCh38
NC_000017.10:g.28546755T>C , CM000679.1:g.28546755T>C	GRCh37
NC_000017.9:g.25570881T>C	NCBI36
NG_011747.2:g.21200A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.344-806A>G MANE Select	ENSP00000498537.1:n.344-806A>G
ENST00000261707.7:c.344-806A>G	ENSP00000261707.3:n.344-806A>G
ENST00000394821.2:c.344-806A>G	ENSP00000378298.2:n.344-806A>G
ENST00000401766.6:c.344-806A>G	ENSP00000385822.2:n.344-806A>G
NM_001045.5:c.344-806A>G	NP_001036.1:n.344-806A>G
NM_001045.6:c.344-806A>G MANE Select	NP_001036.1:n.344-806A>G