Linked Data
MyVariant Identifiers:
chrX:g.154197673A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154969398A>T , CM000685.2:g.154969398A>T | GRCh38 |
| NC_000023.10:g.154197673A>T , CM000685.1:g.154197673A>T | GRCh37 |
| NC_000023.9:g.153850867A>T | NCBI36 |
| NG_011403.1:g.58326T>A | |
| NG_011403.2:g.58326T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.942T>A MANE Select | ENSP00000353393.4:p.Thr314= | |
| ENST00000647125.1:c.*818T>A | ENSP00000496062.1:n.*818T>A | |
| ENST00000360256.8:c.942T>A | ENSP00000353393.4:p.Thr314= | |
| NM_000132.3:c.942T>A | NP_000123.1:p.Thr314= | |
| XM_011531126.1:c.837T>A | XP_011529428.1:p.Thr279= | |
| NM_000132.4:c.942T>A MANE Select | NP_000123.1:p.Thr314= |