MyVariant.info:
GRCh37
chrX:g.153608105G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379745G>C , CM000685.2:g.154379745G>C | GRCh38 |
| NC_000023.10:g.153608105G>C , CM000685.1:g.153608105G>C | GRCh37 |
| NC_000023.9:g.153261299G>C | NCBI36 |
| NG_008677.1:g.10310G>C , LRG_745:g.10310G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682114.1:c.138G>C | ENSP00000507245.1:p.Arg46= | |
| ENST00000682478.1:n.114G>C | ||
| ENST00000683576.1:n.114G>C | ||
| ENST00000683627.1:c.138G>C | ENSP00000507533.1:p.Arg46= | |
| ENST00000684082.1:c.138G>C | ENSP00000508266.1:p.Arg46= | |
| ENST00000684633.1:n.110G>C | ||
| ENST00000684678.1:c.134G>C | ENSP00000507059.1:p.Gly45Ala | |
| ENST00000369842.9:c.138G>C MANE Select | ENSP00000358857.4:p.Arg46= | |
| ENST00000369835.3:c.82+179G>C | ENSP00000358850.3:n.82+179G>C | |
| ENST00000369842.8:c.138G>C | ENSP00000358857.4:p.Arg46= | |
| ENST00000428228.5:c.*43G>C | ENSP00000401081.1:n.*43G>C | |
| ENST00000468294.5:n.98G>C | ||
| ENST00000485261.1:n.163+179G>C | ||
| ENST00000486738.5:n.282G>C | ||
| ENST00000492448.1:n.121G>C | ||
| ENST00000494443.5:n.195G>C | ||
| NM_000117.2:c.138G>C , LRG_745t1:c.138G>C | NP_000108.1:p.Arg46= | |
| XM_024452349.1:c.-71G>C | XP_024308117.1:n.-71G>C | |
| NM_000117.3:c.138G>C MANE Select | NP_000108.1:p.Arg46= |