Linked Data
MyVariant Identifiers:
chrX:g.140983290G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.141895504G>A , CM000685.2:g.141895504G>A | GRCh38 |
| NC_000023.10:g.140983290G>A , CM000685.1:g.140983290G>A | GRCh37 |
| NC_000023.9:g.140810956G>A | NCBI36 |
| NG_013272.1:g.62189G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298296.1:c.1068G>A MANE Select | ENSP00000298296.1:p.Gln356= | |
| ENST00000443323.2:c.-118-927G>A | ENSP00000438254.1:n.-118-927G>A | |
| ENST00000483584.5:n.288+97G>A | ||
| ENST00000544766.5:c.-240+97G>A | ENSP00000440444.1:n.-240+97G>A | |
| NM_138702.1:c.1068G>A MANE Select | NP_619647.1:p.Gln356= | |
| NM_177456.2:c.-240+97G>A | NP_803251.1:n.-240+97G>A | |
| XM_011531267.1:c.-163+97G>A | XP_011529569.1:n.-163+97G>A | |
| XM_011531267.3:c.-163+97G>A | XP_011529569.1:n.-163+97G>A | |
| XM_017029265.2:c.-240+97G>A | XP_016884754.1:n.-240+97G>A |