Linked Data
MyVariant Identifiers:
chrX:g.135741238C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659079C>T , CM000685.2:g.136659079C>T | GRCh38 |
| NC_000023.10:g.135741238C>T , CM000685.1:g.135741238C>T | GRCh37 |
| NC_000023.9:g.135568904C>T | NCBI36 |
| NG_007280.1:g.15903C>T , LRG_141:g.15903C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*68C>T | ENSP00000512122.1:n.*68C>T | |
| ENST00000695725.1:c.*5C>T | ENSP00000512123.1:n.*5C>T | |
| ENST00000695726.1:n.2418C>T | ||
| ENST00000695729.1:n.3253C>T | ||
| ENST00000370629.7:c.450C>T MANE Select | ENSP00000359663.2:p.Asn150= | |
| ENST00000370628.2:c.387C>T | ENSP00000359662.2:p.Asn129= | |
| ENST00000370629.6:c.450C>T | ENSP00000359663.2:p.Asn150= | |
| NM_000074.2:c.450C>T , LRG_141t1:c.450C>T | NP_000065.1:p.Asn150= | |
| NM_000074.3:c.450C>T MANE Select | NP_000065.1:p.Asn150= |