Linked Data
MyVariant Identifiers:
chrX:g.82763626G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83508618G>T , CM000685.2:g.83508618G>T | GRCh38 |
| NC_000023.10:g.82763626G>T , CM000685.1:g.82763626G>T | GRCh37 |
| NC_000023.9:g.82650282G>T | NCBI36 |
| NG_009936.2:g.5358G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644024.2:c.294G>T MANE Select | ENSP00000495996.1:p.Ser98= | |
| ENST00000373200.4:c.294G>T | ENSP00000362296.2:p.Ser98= | |
| NM_000307.4:c.294G>T | NP_000298.3:p.Ser98= | |
| NM_000307.5:c.294G>T MANE Select | NP_000298.3:p.Ser98= |