Linked Data
MyVariant Identifiers:
chrX:g.48385636T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48527248T>C , CM000685.2:g.48527248T>C | GRCh38 |
| NC_000023.10:g.48385636T>C , CM000685.1:g.48385636T>C | GRCh37 |
| NC_000023.9:g.48270580T>C | NCBI36 |
| NG_007452.1:g.10473T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000495186.6:c.432T>C MANE Select | ENSP00000417052.1:p.His144= | |
| ENST00000651615.1:c.432T>C | ENSP00000498524.1:p.His144= | |
| ENST00000276096.10:n.390T>C | ||
| ENST00000414061.1:c.432T>C | ENSP00000405832.1:p.His144= | |
| ENST00000446158.5:c.432T>C | ENSP00000390031.1:p.His144= | |
| ENST00000466461.1:n.271T>C | ||
| ENST00000495186.5:c.432T>C | ENSP00000417052.1:p.His144= | |
| ENST00000498425.1:n.553T>C | ||
| NM_006579.2:c.432T>C | NP_006570.1:p.His144= | |
| NM_006579.3:c.432T>C MANE Select | NP_006570.1:p.His144= |