Linked Data
MyVariant Identifiers:
chrX:g.38535096C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38675842C>G , CM000685.2:g.38675842C>G | GRCh38 |
| NC_000023.10:g.38535096C>G , CM000685.1:g.38535096C>G | GRCh37 |
| NC_000023.9:g.38420040C>G | NCBI36 |
| NG_009160.1:g.119366C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378482.7:c.579C>G MANE Select | ENSP00000367743.2:p.Ala193= | |
| ENST00000286824.6:c.630C>G | ENSP00000286824.6:p.Ala210= | |
| ENST00000378482.6:c.579C>G | ENSP00000367743.2:p.Ala193= | |
| ENST00000419600.3:n.523C>G | ||
| ENST00000465127.1:c.669C>G | ENSP00000417050.1:p.Ala223= | |
| ENST00000471410.5:c.*605C>G | ENSP00000419290.1:n.*605C>G | |
| ENST00000475216.5:c.*572C>G | ENSP00000418586.1:n.*572C>G | |
| NM_004615.3:c.579C>G | NP_004606.2:p.Ala193= | |
| NM_004615.4:c.579C>G MANE Select | NP_004606.2:p.Ala193= |