Linked Data
ClinVar Variation Id:
1972238
ClinVar RCV Id:
RCV002746034
dbSNP Id:
rs750266230
ExAC:
3:43759245 C / A
gnomAD v2:
3-43759245-C-A
gnomAD v4:
3-43717753-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.43717753C>A , CM000665.2:g.43717753C>A | GRCh38 |
| NC_000003.11:g.43759245C>A , CM000665.1:g.43759245C>A | GRCh37 |
| NC_000003.10:g.43734249C>A | NCBI36 |
| NG_007090.3:g.31871C>A | |
| NG_007090.5:g.31884C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000413300.2:c.268-13C>A | ||
| ENST00000454293.2:c.733C>A | ENSP00000412014.2:p.Pro245Thr | |
| ENST00000458276.7:c.774-690C>A | ENSP00000390849.3:n.774-690C>A | |
| ENST00000463153.2:c.83C>A | ||
| ENST00000642351.1:c.733C>A | ENSP00000494478.1:p.Pro245Thr | |
| ENST00000643140.1:c.*218C>A | ENSP00000495588.1:n.*218C>A | |
| ENST00000643477.1:c.*317C>A | ENSP00000496220.1:n.*317C>A | |
| ENST00000643500.1:c.*57C>A | ENSP00000494735.1:n.*57C>A | |
| ENST00000643520.1:n.1022C>A | ||
| ENST00000644371.2:c.856C>A MANE Select | ENSP00000495778.1:p.Pro286Thr | |
| ENST00000646378.1:c.*906C>A | ENSP00000495826.1:n.*906C>A | |
| ENST00000646799.1:c.*248-690C>A | ENSP00000494829.1:n.*248-690C>A | |
| ENST00000649763.1:c.856C>A | ENSP00000497701.1:p.Pro286Thr | |
| ENST00000413300.1:c.270-13C>A | ENSP00000392159.1:n.270-13C>A | |
| ENST00000458276.6:c.856C>A | ENSP00000390849.2:p.Pro286Thr | |
| ENST00000463153.1:n.86C>A | ||
| NM_016006.4:c.856C>A | NP_057090.2:p.Pro286Thr | |
| XM_011533779.1:c.733C>A | XP_011532081.1:p.Pro245Thr | |
| XM_011533780.1:c.774-690C>A | XP_011532082.1:n.774-690C>A | |
| XR_940447.1:n.801C>A | ||
| NM_001355186.1:c.856C>A | NP_001342115.1:p.Pro286Thr | |
| NM_001365649.1:c.733C>A | NP_001352578.1:p.Pro245Thr | |
| NM_001365650.1:c.774-690C>A | NP_001352579.1:n.774-690C>A | |
| NM_016006.5:c.856C>A | NP_057090.2:p.Pro286Thr | |
| NR_158560.1:n.867C>A | ||
| NM_001355186.2:c.856C>A | NP_001342115.1:p.Pro286Thr | |
| NM_016006.6:c.856C>A MANE Select | NP_057090.2:p.Pro286Thr |