Linked Data
MyVariant Identifiers:
chrX:g.29935666A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.29917549A>G , CM000685.2:g.29917549A>G | GRCh38 |
| NC_000023.10:g.29935666A>G , CM000685.1:g.29935666A>G | GRCh37 |
| NC_000023.9:g.29845587A>G | NCBI36 |
| NG_008292.1:g.1334986A>G | |
| NG_008292.2:g.1334986A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378993.6:c.864A>G MANE Select | ENSP00000368278.1:p.Lys288= | |
| ENST00000302196.5:c.87A>G | ENSP00000305200.5:p.Lys29= | |
| ENST00000378993.5:c.864A>G | ENSP00000368278.1:p.Lys288= | |
| NM_014271.3:c.864A>G | NP_055086.1:p.Lys288= | |
| XM_005274441.1:c.864A>G | XP_005274498.1:p.Lys288= | |
| XM_011545445.1:c.864A>G | XP_011543747.1:p.Lys288= | |
| XM_017029240.1:c.864A>G | XP_016884729.1:p.Lys288= | |
| XM_017029241.1:c.486A>G | XP_016884730.1:p.Lys162= | |
| NM_014271.4:c.864A>G MANE Select | NP_055086.1:p.Lys288= |