Linked Data
MyVariant Identifiers:
chrX:g.100601589C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101346601C>A , CM000685.2:g.101346601C>A | GRCh38 |
| NC_000023.10:g.100601589C>A , CM000685.1:g.100601589C>A | GRCh37 |
| NC_000023.9:g.100488245C>A | NCBI36 |
| NG_011734.1:g.7369G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.4:c.192G>T MANE Select | ENSP00000361993.3:p.Val64= | |
| ENST00000644112.2:c.*1786G>T | ENSP00000494385.1:n.*1786G>T | |
| ENST00000645279.1:c.*386G>T | ENSP00000494239.1:n.*386G>T | |
| ENST00000647480.1:n.709G>T | ||
| ENST00000372902.3:c.192G>T | ENSP00000361993.3:p.Val64= | |
| NM_004085.3:c.192G>T | NP_004076.1:p.Val64= | |
| NM_004085.4:c.192G>T MANE Select | NP_004076.1:p.Val64= | |
| NM_001145951.2:c.*1786G>T | NP_001139423.1:n.*1786G>T |