Canonical Allele Identifier: CA289284414

Gene: SLC6A4

Linked Data

• dbSNP Id: rs79255364
• gnomAD v2: 17-28551721-T-C
• gnomAD v3: 17-30224703-T-C
• gnomAD v4: 17-30224703-T-C
• MyVariant Identifiers: chr17:g.28551721T>C (hg19) ; chr17:g.30224703T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30224703T>C , CM000679.2:g.30224703T>C	GRCh38
NC_000017.10:g.28551721T>C , CM000679.1:g.28551721T>C	GRCh37
NC_000017.9:g.25575847T>C	NCBI36
NG_011747.2:g.16234A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650711.1:c.-220-1788A>G MANE Select	ENSP00000498537.1:n.-220-1788A>G
ENST00000261707.7:c.-220-1788A>G	ENSP00000261707.3:n.-220-1788A>G
ENST00000394821.2:c.-220-1788A>G	ENSP00000378298.2:n.-220-1788A>G
ENST00000401766.6:c.-123-2622A>G	ENSP00000385822.2:n.-123-2622A>G
NM_001045.5:c.-220-1788A>G	NP_001036.1:n.-220-1788A>G
NM_001045.6:c.-220-1788A>G MANE Select	NP_001036.1:n.-220-1788A>G