Linked Data
ClinVar Variation Id:
2980271
ClinVar RCV Id:
RCV003837445
dbSNP Id:
rs778043869
ExAC:
4:17493983 T / C
gnomAD v2:
4-17493983-T-C
gnomAD v4:
4-17492360-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.17492360T>C , CM000666.2:g.17492360T>C | GRCh38 |
| NC_000004.11:g.17493983T>C , CM000666.1:g.17493983T>C | GRCh37 |
| NC_000004.10:g.17103081T>C | NCBI36 |
| NG_008763.1:g.24875A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706645.1:n.1484-20A>G | ||
| ENST00000281243.10:c.437-20A>G MANE Select | ENSP00000281243.5:n.437-20A>G | |
| ENST00000281243.9:c.437-20A>G | ENSP00000281243.5:n.437-20A>G | |
| ENST00000428702.6:c.344-20A>G | ENSP00000390944.2:n.344-20A>G | |
| ENST00000501943.6:n.154A>G | ||
| ENST00000505710.1:c.364-1615A>G | ||
| ENST00000507439.5:c.437-1615A>G | ENSP00000423227.1:n.437-1615A>G | |
| ENST00000508623.5:c.437-5124A>G | ENSP00000426377.1:n.437-5124A>G | |
| ENST00000511609.1:n.149A>G | ||
| ENST00000513615.5:c.437-1615A>G | ENSP00000422759.1:n.437-1615A>G | |
| ENST00000514300.1:c.*368-1615A>G | ENSP00000426039.1:n.*368-1615A>G | |
| NM_000320.2:c.437-20A>G | NP_000311.2:n.437-20A>G | |
| NM_001306140.1:c.344-20A>G | NP_001293069.1:n.344-20A>G | |
| XR_241677.1:n.600-1615A>G | ||
| NR_156494.1:n.617-1615A>G | ||
| NM_000320.3:c.437-20A>G MANE Select | NP_000311.2:n.437-20A>G | |
| NM_001306140.2:c.344-20A>G | NP_001293069.1:n.344-20A>G | |
| NR_156494.2:n.473-1615A>G |