Linked Data
MyVariant Identifiers:
chrX:g.82763443T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83508435T>G , CM000685.2:g.83508435T>G | GRCh38 |
| NC_000023.10:g.82763443T>G , CM000685.1:g.82763443T>G | GRCh37 |
| NC_000023.9:g.82650099T>G | NCBI36 |
| NG_009936.2:g.5175T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644024.2:c.111T>G MANE Select | ENSP00000495996.1:p.Leu37= | |
| ENST00000373200.4:c.111T>G | ENSP00000362296.2:p.Leu37= | |
| NM_000307.4:c.111T>G | NP_000298.3:p.Leu37= | |
| NM_000307.5:c.111T>G MANE Select | NP_000298.3:p.Leu37= |