Linked Data
MyVariant Identifiers:
chrX:g.50658842C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50915842C>G , CM000685.2:g.50915842C>G | GRCh38 |
| NC_000023.10:g.50658842C>G , CM000685.1:g.50658842C>G | GRCh37 |
| NC_000023.9:g.50675582C>G | NCBI36 |
| NG_012894.1:g.10059C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.414C>G MANE Select | ENSP00000252677.3:p.Arg138= | |
| ENST00000252677.3:c.414C>G | ENSP00000252677.3:p.Arg138= | |
| NM_005448.2:c.414C>G MANE Select | NP_005439.2:p.Arg138= |