Linked Data
MyVariant Identifiers:
chrX:g.115303542C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116172289C>G , CM000685.2:g.116172289C>G | GRCh38 |
| NC_000023.10:g.115303542C>G , CM000685.1:g.115303542C>G | GRCh37 |
| NC_000023.9:g.115217570C>G | NCBI36 |
| NG_016326.1:g.6585C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.9C>G MANE Select | ENSP00000360973.4:p.Gly3= | |
| ENST00000680409.1:n.477C>G | ||
| ENST00000681852.1:c.9C>G | ENSP00000505750.1:p.Gly3= | |
| ENST00000371906.4:c.9C>G | ENSP00000360973.4:p.Gly3= | |
| NM_000686.4:c.9C>G | NP_000677.2:p.Gly3= | |
| XM_011537533.1:c.9C>G | XP_011535835.1:p.Gly3= | |
| NM_000686.5:c.9C>G MANE Select | NP_000677.2:p.Gly3= | |
| NM_001385624.1:c.9C>G | NP_001372553.1:p.Gly3= |