Linked Data
ClinVar Variation Id:
234655
ClinVar RCV Id:
RCV000221876
dbSNP Id:
rs147622433
ExAC:
1:197073959 C / T
gnomAD v2:
1-197073959-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197104829C>T , CM000663.2:g.197104829C>T | GRCh38 |
| NC_000001.10:g.197073959C>T , CM000663.1:g.197073959C>T | GRCh37 |
| NC_000001.9:g.195340582C>T | NCBI36 |
| NG_015867.1:g.46866G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367408.6:n.2108-8665G>A | ||
| ENST00000367409.9:c.4422G>A MANE Select | ENSP00000356379.4:p.Trp1474Ter | |
| ENST00000680265.1:c.4422G>A | ENSP00000505384.1:p.Trp1474Ter | |
| ENST00000680710.1:c.4422G>A | ENSP00000506676.1:p.Trp1474Ter | |
| ENST00000681879.1:c.4470G>A | ENSP00000505363.1:n.4470G>A | |
| ENST00000294732.11:c.4066-8665G>A | ENSP00000294732.7:n.4066-8665G>A | |
| ENST00000367408.5:c.1816-8665G>A | ENSP00000356378.1:n.1816-8665G>A | |
| ENST00000367409.8:c.4422G>A | ENSP00000356379.4:p.Trp1474Ter | |
| ENST00000612785.1:c.562-2182G>A | ENSP00000479244.1:n.562-2182G>A | |
| NM_001206846.1:c.4066-8665G>A | NP_001193775.1:n.4066-8665G>A | |
| NM_018136.4:c.4422G>A | NP_060606.3:p.Trp1474Ter | |
| NM_018136.5:c.4422G>A MANE Select | NP_060606.3:p.Trp1474Ter | |
| NM_001206846.2:c.4066-8665G>A | NP_001193775.1:n.4066-8665G>A |