Linked Data
MyVariant Identifiers:
chrX:g.135741256A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659097A>G , CM000685.2:g.136659097A>G | GRCh38 |
| NC_000023.10:g.135741256A>G , CM000685.1:g.135741256A>G | GRCh37 |
| NC_000023.9:g.135568922A>G | NCBI36 |
| NG_007280.1:g.15921A>G , LRG_141:g.15921A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695724.1:c.*86A>G | ENSP00000512122.1:n.*86A>G | |
| ENST00000695725.1:c.*23A>G | ENSP00000512123.1:n.*23A>G | |
| ENST00000695726.1:n.2436A>G | ||
| ENST00000695729.1:n.3271A>G | ||
| ENST00000370629.7:c.468A>G MANE Select | ENSP00000359663.2:p.Glu156= | |
| ENST00000370628.2:c.405A>G | ENSP00000359662.2:p.Glu135= | |
| ENST00000370629.6:c.468A>G | ENSP00000359663.2:p.Glu156= | |
| NM_000074.2:c.468A>G , LRG_141t1:c.468A>G | NP_000065.1:p.Glu156= | |
| NM_000074.3:c.468A>G MANE Select | NP_000065.1:p.Glu156= |