ClinVar RCV:
ClinVar Variation:
COSMIC:
dbSNP:
gnomAD v4:
Joint Max Group AF
0.00000875 (SAS)
Exomes Max Group AF
0.00000924 (SAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197104519G>A , CM000663.2:g.197104519G>A | GRCh38 |
| NC_000001.10:g.197073649G>A , CM000663.1:g.197073649G>A | GRCh37 |
| NC_000001.9:g.195340272G>A | NCBI36 |
| NG_015867.1:g.47176C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367408.6:n.2108-8355C>T | ||
| ENST00000367409.9:c.4732C>T MANE Select | ENSP00000356379.4:p.Arg1578Ter | |
| ENST00000680265.1:c.4732C>T | ENSP00000505384.1:p.Arg1578Ter | |
| ENST00000680710.1:c.4732C>T | ENSP00000506676.1:p.Arg1578Ter | |
| ENST00000294732.11:c.4066-8355C>T | ENSP00000294732.7:n.4066-8355C>T | |
| ENST00000367408.5:c.1816-8355C>T | ENSP00000356378.1:n.1816-8355C>T | |
| ENST00000367409.8:c.4732C>T | ENSP00000356379.4:p.Arg1578Ter | |
| ENST00000612785.1:c.562-1872C>T | ENSP00000479244.1:n.562-1872C>T | |
| NM_001206846.1:c.4066-8355C>T | NP_001193775.1:n.4066-8355C>T | |
| NM_018136.4:c.4732C>T | NP_060606.3:p.Arg1578Ter | |
| NM_018136.5:c.4732C>T MANE Select | NP_060606.3:p.Arg1578Ter | |
| NM_001206846.2:c.4066-8355C>T | NP_001193775.1:n.4066-8355C>T |