Linked Data
dbSNP Id:
rs782464092
gnomAD v2:
X-152954298-T-A
MyVariant Identifiers:
chrX:g.152954298T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153688843T>A , CM000685.2:g.153688843T>A | GRCh38 |
| NC_000023.10:g.152954298T>A , CM000685.1:g.152954298T>A | GRCh37 |
| NC_000023.9:g.152607492T>A | NCBI36 |
| NG_012016.1:g.5547T>A | |
| NG_012016.2:g.5547T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000253122.10:c.262+7T>A (SLC6A8) MANE Select | ENSP00000253122.5:n.262+7T>A | |
| ENST00000253122.9:c.262+7T>A (SLC6A8) | ENSP00000253122.5:n.262+7T>A | |
| ENST00000458354.5:c.-31A>T (PNCK) | ENSP00000401542.1:n.-31A>T | |
| ENST00000476466.1:n.114+7T>A (SLC6A8) | ||
| ENST00000480693.1:n.36A>T (PNCK) | ||
| NM_001142805.1:c.262+7T>A (SLC6A8) | NP_001136277.1:n.262+7T>A | |
| NM_005629.3:c.262+7T>A (SLC6A8) | NP_005620.1:n.262+7T>A | |
| NM_005629.4:c.262+7T>A (SLC6A8) MANE Select | NP_005620.1:n.262+7T>A | |
| NM_001142805.2:c.262+7T>A (SLC6A8) | NP_001136277.1:n.262+7T>A |