Linked Data
MyVariant Identifiers:
chrX:g.100603614A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348626A>T , CM000685.2:g.101348626A>T | GRCh38 |
| NC_000023.10:g.100603614A>T , CM000685.1:g.100603614A>T | GRCh37 |
| NC_000023.9:g.100490270A>T | NCBI36 |
| NG_009616.1:g.42599T>A , LRG_128:g.42599T>A | |
| NG_011734.1:g.5344T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.4:c.39T>A MANE Select | ENSP00000361993.3:p.Gly13= | |
| ENST00000644112.2:c.39T>A | ENSP00000494385.1:p.Gly13= | |
| ENST00000645279.1:c.39T>A | ENSP00000494239.1:p.Gly13= | |
| ENST00000372902.3:c.39T>A | ENSP00000361993.3:p.Gly13= | |
| ENST00000480575.1:n.124T>A | ||
| NM_001145951.1:c.39T>A | NP_001139423.1:p.Gly13= | |
| NM_004085.3:c.39T>A | NP_004076.1:p.Gly13= | |
| NM_004085.4:c.39T>A MANE Select | NP_004076.1:p.Gly13= | |
| NM_001145951.2:c.39T>A | NP_001139423.1:p.Gly13= |