Linked Data
ClinVar Variation Id:
1323838
ClinVar RCV Id:
RCV001780637
dbSNP Id:
rs370301465
gnomAD v4:
3-43717735-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.43717735C>T , CM000665.2:g.43717735C>T | GRCh38 |
| NC_000003.11:g.43759227C>T , CM000665.1:g.43759227C>T | GRCh37 |
| NC_000003.10:g.43734231C>T | NCBI36 |
| NG_007090.3:g.31853C>T | |
| NG_007090.5:g.31866C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000413300.2:c.268-31C>T | ||
| ENST00000454293.2:c.715C>T | ENSP00000412014.2:p.Arg239Ter | |
| ENST00000458276.7:c.774-708C>T | ENSP00000390849.3:n.774-708C>T | |
| ENST00000463153.2:c.65C>T | ||
| ENST00000642351.1:c.715C>T | ENSP00000494478.1:p.Arg239Ter | |
| ENST00000643140.1:c.*200C>T | ENSP00000495588.1:n.*200C>T | |
| ENST00000643477.1:c.*299C>T | ENSP00000496220.1:n.*299C>T | |
| ENST00000643500.1:c.*39C>T | ENSP00000494735.1:n.*39C>T | |
| ENST00000643520.1:n.1004C>T | ||
| ENST00000644371.2:c.838C>T MANE Select | ENSP00000495778.1:p.Arg280Ter | |
| ENST00000646378.1:c.*888C>T | ENSP00000495826.1:n.*888C>T | |
| ENST00000646799.1:c.*248-708C>T | ENSP00000494829.1:n.*248-708C>T | |
| ENST00000649763.1:c.838C>T | ENSP00000497701.1:p.Arg280Ter | |
| ENST00000413300.1:c.270-31C>T | ENSP00000392159.1:n.270-31C>T | |
| ENST00000458276.6:c.838C>T | ENSP00000390849.2:p.Arg280Ter | |
| ENST00000463153.1:n.68C>T | ||
| NM_016006.4:c.838C>T | NP_057090.2:p.Arg280Ter | |
| XM_011533779.1:c.715C>T | XP_011532081.1:p.Arg239Ter | |
| XM_011533780.1:c.774-708C>T | XP_011532082.1:n.774-708C>T | |
| XR_940447.1:n.783C>T | ||
| NM_001355186.1:c.838C>T | NP_001342115.1:p.Arg280Ter | |
| NM_001365649.1:c.715C>T | NP_001352578.1:p.Arg239Ter | |
| NM_001365650.1:c.774-708C>T | NP_001352579.1:n.774-708C>T | |
| NM_016006.5:c.838C>T | NP_057090.2:p.Arg280Ter | |
| NR_158560.1:n.849C>T | ||
| NM_001355186.2:c.838C>T | NP_001342115.1:p.Arg280Ter | |
| NM_016006.6:c.838C>T MANE Select | NP_057090.2:p.Arg280Ter |