Linked Data
MyVariant Identifiers:
chrX:g.154156902T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154928627T>C , CM000685.2:g.154928627T>C | GRCh38 |
| NC_000023.10:g.154156902T>C , CM000685.1:g.154156902T>C | GRCh37 |
| NC_000023.9:g.153810096T>C | NCBI36 |
| NG_011403.1:g.99097A>G | |
| NG_011403.2:g.99097A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5163A>G MANE Select | ENSP00000353393.4:p.Ala1721= | |
| ENST00000360256.8:c.5163A>G | ENSP00000353393.4:p.Ala1721= | |
| NM_000132.3:c.5163A>G | NP_000123.1:p.Ala1721= | |
| XM_011531126.1:c.5058A>G | XP_011529428.1:p.Ala1686= | |
| NM_000132.4:c.5163A>G MANE Select | NP_000123.1:p.Ala1721= |