Linked Data
ClinVar Variation Id:
1573438
ClinVar RCV Id:
RCV002216043
dbSNP Id:
rs2147052123
MyVariant Identifiers:
chrX:g.13779211C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.13761092C>G , CM000685.2:g.13761092C>G | GRCh38 |
| NC_000023.10:g.13779211C>G , CM000685.1:g.13779211C>G | GRCh37 |
| NC_000023.9:g.13689132C>G | NCBI36 |
| NG_008872.1:g.31380C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380567.6:c.*1961C>G | ENSP00000369941.2:n.*1961C>G | |
| ENST00000398395.8:c.*1729C>G | ENSP00000381432.5:n.*1729C>G | |
| ENST00000464463.6:n.4097C>G | ||
| ENST00000490265.6:n.2797C>G | ||
| ENST00000682237.1:c.*1828C>G | ENSP00000507121.1:n.*1828C>G | |
| ENST00000682562.1:c.*3670C>G | ENSP00000507874.1:n.*3670C>G | |
| ENST00000682953.1:c.*2995C>G | ENSP00000507878.1:n.*2995C>G | |
| ENST00000683055.1:c.*3249C>G | ENSP00000508191.1:n.*3249C>G | |
| ENST00000683284.1:c.*2499C>G | ENSP00000507837.1:n.*2499C>G | |
| ENST00000683427.1:c.*925C>G | ENSP00000507290.1:n.*925C>G | |
| ENST00000683454.1:n.2282C>G | ||
| ENST00000683637.1:n.3377C>G | ||
| ENST00000683655.1:c.*2482C>G | ENSP00000506770.1:n.*2482C>G | |
| ENST00000683713.1:c.*2499C>G | ENSP00000507797.1:n.*2499C>G | |
| ENST00000684577.1:c.*1965C>G | ENSP00000507871.1:n.*1965C>G | |
| ENST00000340096.11:c.2268C>G MANE Select | ENSP00000344314.6:p.Gly756= | |
| ENST00000340096.10:c.2268C>G | ENSP00000344314.6:p.Gly756= | |
| ENST00000380550.6:c.2148C>G | ENSP00000369923.3:p.Gly716= | |
| ENST00000380567.5:c.1848C>G | ENSP00000369941.1:p.Gly616= | |
| ENST00000398395.7:c.*608C>G | ENSP00000381432.4:n.*608C>G | |
| ENST00000464463.5:n.89C>G | ||
| ENST00000490265.5:n.3243C>G | ||
| NM_003611.2:c.2268C>G | NP_003602.1:p.Gly756= | |
| XM_005274599.2:c.2289C>G | XP_005274656.1:p.Gly763= | |
| XM_005274602.2:c.2289C>G | XP_005274659.1:p.Gly763= | |
| XM_005274603.2:c.2169C>G | XP_005274660.1:p.Gly723= | |
| XM_005274604.2:c.2148C>G | XP_005274661.1:p.Gly716= | |
| XM_005274606.2:c.2124C>G | XP_005274663.1:p.Gly708= | |
| XM_005274607.3:c.1848C>G | XP_005274664.1:p.Gly616= | |
| XM_011545591.1:c.2289C>G | XP_011543893.1:p.Gly763= | |
| XM_011545592.1:c.2076C>G | XP_011543894.1:p.Gly692= | |
| XM_011545593.1:c.2289C>G | XP_011543895.1:p.Gly763= | |
| XM_011545594.1:c.1947C>G | XP_011543896.1:p.Gly649= | |
| XM_011545595.1:c.1947C>G | XP_011543897.1:p.Gly649= | |
| XM_011545596.1:c.2289C>G | XP_011543898.1:p.Gly763= | |
| XM_011545597.1:c.1848C>G | XP_011543899.1:p.Gly616= | |
| XM_011545598.1:c.993C>G | XP_011543900.1:p.Gly331= | |
| XR_247288.2:n.2628C>G | ||
| NM_001330209.1:c.2148C>G | NP_001317138.1:p.Gly716= | |
| NM_001330210.1:c.1848C>G | NP_001317139.1:p.Gly616= | |
| XM_005274606.4:c.2124C>G | XP_005274663.1:p.Gly708= | |
| XM_011545592.3:c.2076C>G | XP_011543894.1:p.Gly692= | |
| XM_011545594.3:c.1947C>G | XP_011543896.1:p.Gly649= | |
| XM_011545597.2:c.1848C>G | XP_011543899.1:p.Gly616= | |
| XM_017029909.1:c.1848C>G | XP_016885398.1:p.Gly616= | |
| XM_017029911.1:c.1326C>G | XP_016885400.1:p.Gly442= | |
| XM_024452468.1:c.993C>G | XP_024308236.1:p.Gly331= | |
| XM_024452469.1:c.993C>G | XP_024308237.1:p.Gly331= | |
| XM_024452470.1:c.993C>G | XP_024308238.1:p.Gly331= | |
| XM_024452471.1:c.993C>G | XP_024308239.1:p.Gly331= | |
| NM_003611.3:c.2268C>G MANE Select | NP_003602.1:p.Gly756= | |
| NM_001330209.2:c.2148C>G | NP_001317138.1:p.Gly716= | |
| NM_001330210.2:c.1848C>G | NP_001317139.1:p.Gly616= |