Linked Data
MyVariant Identifiers:
chrX:g.37587160T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37727907T>G , CM000685.2:g.37727907T>G | GRCh38 |
| NC_000023.10:g.37587160T>G , CM000685.1:g.37587160T>G | GRCh37 |
| NC_000023.9:g.37472099T>G | NCBI36 |
| NG_007473.1:g.47048T>G | |
| NG_007473.3:g.47028T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378616.5:c.780T>G MANE Select | ENSP00000367879.3:p.Gly260= | |
| ENST00000378616.3:c.780T>G | ENSP00000367879.3:p.Gly260= | |
| ENST00000465127.1:c.171+301907T>G | ENSP00000417050.1:n.171+301907T>G | |
| NM_021083.2:c.780T>G | NP_066569.1:p.Gly260= | |
| NM_021083.4:c.780T>G MANE Select | NP_066569.1:p.Gly260= |