Linked Data
ClinVar Variation Id:
189773
dbSNP Id:
rs786205045
gnomAD v4:
X-154097618-G-A
PubMed:
PMID:23866855
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097618G>A , CM000685.2:g.154097618G>A | GRCh38 |
| NC_000023.10:g.153363075G>A , CM000685.1:g.153363075G>A | GRCh37 |
| NC_000023.9:g.153016269G>A | NCBI36 |
| NG_007107.2:g.44504C>T | |
| NG_007107.3:g.44486C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700484.1:n.8C>T | ||
| ENST00000303391.11:c.-113C>T MANE Plus Clinical | ENSP00000301948.6:n.-113C>T | |
| ENST00000453960.7:c.48C>T MANE Select | ENSP00000395535.2:p.Gly16= | |
| ENST00000676382.1:n.8C>T | ||
| ENST00000303391.10:c.-113C>T | ENSP00000301948.6:n.-113C>T | |
| ENST00000369957.5:c.-113C>T | ENSP00000358973.4:n.-113C>T | |
| ENST00000407218.5:c.48C>T | ENSP00000384865.2:p.Gly16= | |
| ENST00000453960.6:c.48C>T | ENSP00000395535.2:p.Gly16= | |
| ENST00000619732.4:c.-113C>T | ENSP00000480973.1:n.-113C>T | |
| ENST00000627864.1:n.63C>T | ||
| ENST00000628176.2:c.-113C>T | ENSP00000486978.1:n.-113C>T | |
| ENST00000631210.1:n.305+7163C>T | ||
| NM_001110792.1:c.48C>T | NP_001104262.1:p.Gly16= | |
| NM_001316337.1:c.-560C>T | NP_001303266.1:n.-560C>T | |
| NM_004992.3:c.-113C>T | NP_004983.1:n.-113C>T | |
| XM_005274682.3:c.-504C>T | XP_005274739.1:n.-504C>T | |
| NM_001110792.2:c.48C>T MANE Select | NP_001104262.1:p.Gly16= | |
| NM_001316337.2:c.-560C>T | NP_001303266.1:n.-560C>T | |
| NM_001369391.2:c.-855C>T | NP_001356320.1:n.-855C>T | |
| NM_001369392.2:c.-504C>T | NP_001356321.1:n.-504C>T | |
| NM_001369393.2:c.-380C>T | NP_001356322.1:n.-380C>T | |
| NM_001386137.1:c.-785C>T | NP_001373066.1:n.-785C>T | |
| NM_001386138.1:c.-673C>T | NP_001373067.1:n.-673C>T | |
| NM_001386139.1:c.-549C>T | NP_001373068.1:n.-549C>T | |
| NM_004992.4:c.-113C>T MANE Plus Clinical | NP_004983.1:n.-113C>T |