Linked Data
MyVariant Identifiers:
chrX:g.73641886A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.74422051A>G , CM000685.2:g.74422051A>G | GRCh38 |
| NC_000023.10:g.73641886A>G , CM000685.1:g.73641886A>G | GRCh37 |
| NC_000023.9:g.73558611A>G | NCBI36 |
| NG_011641.1:g.5802A>G | |
| NG_011641.2:g.5802A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000587091.6:c.414A>G MANE Select | ENSP00000465734.1:p.Gln138= | |
| ENST00000636771.1:c.160A>G | ||
| ENST00000587091.5:c.414A>G | ENSP00000465734.1:p.Gln138= | |
| NM_006517.4:c.414A>G | NP_006508.2:p.Gln138= | |
| XM_005262294.1:c.414A>G | XP_005262351.1:p.Gln138= | |
| XM_011531015.1:c.414A>G | XP_011529317.1:p.Gln138= | |
| NM_006517.5:c.414A>G MANE Select | NP_006508.2:p.Gln138= |