Linked Data
ClinVar Variation Id:
2080794
ClinVar RCV Id:
RCV003002197
dbSNP Id:
rs1490669105
gnomAD v2:
10-50819849-C-G
gnomAD v4:
10-49611803-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49611803C>G , CM000672.2:g.49611803C>G | GRCh38 |
| NC_000010.10:g.50819849C>G , CM000672.1:g.50819849C>G | GRCh37 |
| NC_000010.9:g.50489855C>G | NCBI36 |
| NG_011797.1:g.7709C>G | |
| NG_053144.1:g.6503C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374115.5:c.1063C>G (SLC18A3) MANE Select | ENSP00000363229.3:p.Leu355Val | |
| ENST00000339797.5:c.-69+2604C>G (CHAT) | ENSP00000343486.1:n.-69+2604C>G | |
| ENST00000374115.4:c.1063C>G (SLC18A3) | ENSP00000363229.3:p.Leu355Val | |
| NM_003055.2:c.1063C>G (SLC18A3) | NP_003046.2:p.Leu355Val | |
| NM_020984.3:c.-69+2604C>G (CHAT) | NP_066264.3:n.-69+2604C>G | |
| NM_003055.3:c.1063C>G (SLC18A3) MANE Select | NP_003046.2:p.Leu355Val | |
| NM_020984.4:c.-69+2604C>G (CHAT) | NP_066264.4:n.-69+2604C>G |