Canonical Allele Identifier: CA10639310
Gene: SLC6A4 HGNC NCBI
MyVariant.info:
GRCh38 chr17:g.30197786A>C
GRCh37 chr17:g.28524804A>C
gnomAD v2:
17:28524804 A / C
gnomAD v3:
17:30197786 A / C
gnomAD v4:
chr17-30197786-A-C
Joint Max Group AF 0.78261556 (EAS)
Genomes Max Group AF 0.79436225 (EAS)
Exomes Max Group AF 0.29345167 (NFE)
ClinVar RCV:
RCV000302486
ClinVar Variation:
322518
dbSNP:
3813034
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30197786A>C , CM000679.2:g.30197786A>C GRCh38
NC_000017.10:g.28524804A>C , CM000679.1:g.28524804A>C GRCh37
NC_000017.9:g.25548930A>C NCBI36
NG_011747.2:g.43151T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.*670T>G MANE Select ENSP00000498537.1:n.*670T>G
ENST00000261707.7:c.*670T>G ENSP00000261707.3:n.*670T>G
ENST00000401766.6:c.*670T>G ENSP00000385822.2:n.*670T>G
NM_001045.5:c.*670T>G NP_001036.1:n.*670T>G
NM_001045.6:c.*670T>G MANE Select NP_001036.1:n.*670T>G
Search 100 bp 5'
Search 100 bp 3'