Linked Data
MyVariant Identifiers:
chrX:g.50659217C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50916217C>A , CM000685.2:g.50916217C>A | GRCh38 |
| NC_000023.10:g.50659217C>A , CM000685.1:g.50659217C>A | GRCh37 |
| NC_000023.9:g.50675957C>A | NCBI36 |
| NG_012894.1:g.10434C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.789C>A MANE Select | ENSP00000252677.3:p.Leu263= | |
| ENST00000252677.3:c.789C>A | ENSP00000252677.3:p.Leu263= | |
| NM_005448.2:c.789C>A MANE Select | NP_005439.2:p.Leu263= |