Linked Data
MyVariant Identifiers:
chrX:g.153001618G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736164G>T , CM000685.2:g.153736164G>T | GRCh38 |
| NC_000023.10:g.153001618G>T , CM000685.1:g.153001618G>T | GRCh37 |
| NC_000023.9:g.152654812G>T | NCBI36 |
| NG_009022.2:g.16297G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1134G>T MANE Select | ENSP00000218104.3:p.Val378= | |
| ENST00000218104.5:c.1134G>T | ENSP00000218104.3:p.Val378= | |
| ENST00000443684.2:n.137G>T | ||
| NM_000033.3:c.1134G>T | NP_000024.2:p.Val378= | |
| XR_938507.1:n.1550G>T | ||
| XR_938507.2:n.1550G>T | ||
| NM_000033.4:c.1134G>T MANE Select | NP_000024.2:p.Val378= |