Linked Data
ClinVar Variation Id:
435812
dbSNP Id:
rs748344922
ExAC:
X:43571142 C / T
gnomAD v2:
X-43571142-C-T
gnomAD v3:
X-43711895-C-T
gnomAD v4:
X-43711895-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.43711895C>T , CM000685.2:g.43711895C>T | GRCh38 |
| NC_000023.10:g.43571142C>T , CM000685.1:g.43571142C>T | GRCh37 |
| NC_000023.9:g.43456086C>T | NCBI36 |
| NG_008957.2:g.60735C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000542639.6:c.-70C>T | ENSP00000440846.1:n.-70C>T | |
| ENST00000686683.1:c.-281C>T | ENSP00000509063.1:n.-281C>T | |
| ENST00000686980.1:n.462C>T | ||
| ENST00000688006.1:c.-70C>T | ENSP00000510311.1:n.-70C>T | |
| ENST00000689087.1:c.-70C>T | ENSP00000508997.1:n.-70C>T | |
| ENST00000693128.1:c.307-810C>T | ENSP00000508493.1:n.307-810C>T | |
| ENST00000338702.4:c.330C>T MANE Select | ENSP00000340684.3:p.Gly110= | |
| ENST00000338702.3:c.330C>T | ENSP00000340684.3:p.Gly110= | |
| ENST00000497485.1:n.478C>T | ||
| ENST00000542639.5:c.-70C>T | ENSP00000440846.1:n.-70C>T | |
| NM_000240.3:c.330C>T | NP_000231.1:p.Gly110= | |
| NM_001270458.1:c.-70C>T | NP_001257387.1:n.-70C>T | |
| NM_000240.4:c.330C>T MANE Select | NP_000231.1:p.Gly110= | |
| NM_001270458.2:c.-70C>T | NP_001257387.1:n.-70C>T |