MyVariant.info:
GRCh37
chrX:g.140983129A>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.141895343A>T , CM000685.2:g.141895343A>T | GRCh38 |
| NC_000023.10:g.140983129A>T , CM000685.1:g.140983129A>T | GRCh37 |
| NC_000023.9:g.140810795A>T | NCBI36 |
| NG_013272.1:g.62028A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298296.1:c.984A>T MANE Select | ENSP00000298296.1:p.Ala328= | |
| ENST00000443323.2:c.-118-1088A>T | ENSP00000438254.1:n.-118-1088A>T | |
| ENST00000483584.5:n.224A>T | ||
| ENST00000544766.5:c.-304A>T | ENSP00000440444.1:n.-304A>T | |
| NM_138702.1:c.984A>T MANE Select | NP_619647.1:p.Ala328= | |
| NM_177456.2:c.-304A>T | NP_803251.1:n.-304A>T | |
| XM_011531267.1:c.-227A>T | XP_011529569.1:n.-227A>T | |
| XM_011531267.3:c.-227A>T | XP_011529569.1:n.-227A>T | |
| XM_017029265.2:c.-304A>T | XP_016884754.1:n.-304A>T |