Linked Data
MyVariant Identifiers:
chrX:g.29417358A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.29399241A>T , CM000685.2:g.29399241A>T | GRCh38 |
| NC_000023.10:g.29417358A>T , CM000685.1:g.29417358A>T | GRCh37 |
| NC_000023.9:g.29327279A>T | NCBI36 |
| NG_008292.1:g.816678A>T | |
| NG_008292.2:g.816678A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378993.6:c.636A>T MANE Select | ENSP00000368278.1:p.Gly212= | |
| ENST00000378993.5:c.636A>T | ENSP00000368278.1:p.Gly212= | |
| NM_014271.3:c.636A>T | NP_055086.1:p.Gly212= | |
| XM_005274441.1:c.636A>T | XP_005274498.1:p.Gly212= | |
| XM_011545445.1:c.636A>T | XP_011543747.1:p.Gly212= | |
| XM_017029240.1:c.636A>T | XP_016884729.1:p.Gly212= | |
| XM_017029241.1:c.258A>T | XP_016884730.1:p.Gly86= | |
| NM_014271.4:c.636A>T MANE Select | NP_055086.1:p.Gly212= |