Linked Data
MyVariant Identifiers:
chrX:g.115303800T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116172547T>G , CM000685.2:g.116172547T>G | GRCh38 |
| NC_000023.10:g.115303800T>G , CM000685.1:g.115303800T>G | GRCh37 |
| NC_000023.9:g.115217828T>G | NCBI36 |
| NG_016326.1:g.6843T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.267T>G MANE Select | ENSP00000360973.4:p.Ala89= | |
| ENST00000680409.1:n.735T>G | ||
| ENST00000681852.1:c.267T>G | ENSP00000505750.1:p.Ala89= | |
| ENST00000371906.4:c.267T>G | ENSP00000360973.4:p.Ala89= | |
| NM_000686.4:c.267T>G | NP_000677.2:p.Ala89= | |
| XM_011537533.1:c.267T>G | XP_011535835.1:p.Ala89= | |
| NM_000686.5:c.267T>G MANE Select | NP_000677.2:p.Ala89= | |
| NM_001385624.1:c.267T>G | NP_001372553.1:p.Ala89= |