Linked Data
dbSNP Id:
rs1304017330
gnomAD v2:
X-152954378-T-G
gnomAD v3:
X-153688923-T-G
gnomAD v4:
X-153688923-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153688923T>G , CM000685.2:g.153688923T>G | GRCh38 |
| NC_000023.10:g.152954378T>G , CM000685.1:g.152954378T>G | GRCh37 |
| NC_000023.9:g.152607572T>G | NCBI36 |
| NG_012016.1:g.5627T>G | |
| NG_012016.2:g.5627T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.262+87T>G (SLC6A8) MANE Select | ENSP00000253122.5:n.262+87T>G | |
| ENST00000253122.9:c.262+87T>G (SLC6A8) | ENSP00000253122.5:n.262+87T>G | |
| ENST00000458354.5:c.-111A>C (PNCK) | ENSP00000401542.1:n.-111A>C | |
| ENST00000476466.1:n.114+87T>G (SLC6A8) | ||
| NM_001142805.1:c.262+87T>G (SLC6A8) | NP_001136277.1:n.262+87T>G | |
| NM_005629.3:c.262+87T>G (SLC6A8) | NP_005620.1:n.262+87T>G | |
| NM_005629.4:c.262+87T>G (SLC6A8) MANE Select | NP_005620.1:n.262+87T>G | |
| NM_001142805.2:c.262+87T>G (SLC6A8) | NP_001136277.1:n.262+87T>G |