Linked Data
MyVariant Identifiers:
chrX:g.73641766C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.74421931C>T , CM000685.2:g.74421931C>T | GRCh38 |
| NC_000023.10:g.73641766C>T , CM000685.1:g.73641766C>T | GRCh37 |
| NC_000023.9:g.73558491C>T | NCBI36 |
| NG_011641.1:g.5682C>T | |
| NG_011641.2:g.5682C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000587091.6:c.294C>T MANE Select | ENSP00000465734.1:p.Gly98= | |
| ENST00000636771.1:c.40C>T | ||
| ENST00000587091.5:c.294C>T | ENSP00000465734.1:p.Gly98= | |
| NM_006517.4:c.294C>T | NP_006508.2:p.Gly98= | |
| XM_005262294.1:c.294C>T | XP_005262351.1:p.Gly98= | |
| XM_011531015.1:c.294C>T | XP_011529317.1:p.Gly98= | |
| NM_006517.5:c.294C>T MANE Select | NP_006508.2:p.Gly98= |