Linked Data
MyVariant Identifiers:
chrX:g.135741262G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659103G>C , CM000685.2:g.136659103G>C | GRCh38 |
| NC_000023.10:g.135741262G>C , CM000685.1:g.135741262G>C | GRCh37 |
| NC_000023.9:g.135568928G>C | NCBI36 |
| NG_007280.1:g.15927G>C , LRG_141:g.15927G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695724.1:c.*92G>C | ENSP00000512122.1:n.*92G>C | |
| ENST00000695725.1:c.*29G>C | ENSP00000512123.1:n.*29G>C | |
| ENST00000695726.1:n.2442G>C | ||
| ENST00000695729.1:n.3277G>C | ||
| ENST00000370629.7:c.474G>C MANE Select | ENSP00000359663.2:p.Gly158= | |
| ENST00000370628.2:c.411G>C | ENSP00000359662.2:p.Gly137= | |
| ENST00000370629.6:c.474G>C | ENSP00000359663.2:p.Gly158= | |
| NM_000074.2:c.474G>C , LRG_141t1:c.474G>C | NP_000065.1:p.Gly158= | |
| NM_000074.3:c.474G>C MANE Select | NP_000065.1:p.Gly158= |