Linked Data
ClinVar Variation Id:
459868
dbSNP Id:
rs201971114
ExAC:
2:73677970 A / C
gnomAD v2:
2-73677970-A-C
gnomAD v3:
2-73450843-A-C
gnomAD v4:
2-73450843-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73450843A>C , CM000664.2:g.73450843A>C | GRCh38 |
| NC_000002.11:g.73677970A>C , CM000664.1:g.73677970A>C | GRCh37 |
| NC_000002.10:g.73531478A>C | NCBI36 |
| NG_011690.1:g.70091A>C , LRG_741:g.70091A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682565.1:c.3935A>C | ENSP00000507671.1:p.Tyr1312Ser | |
| ENST00000682801.1:c.3935A>C | ENSP00000507862.1:p.Tyr1312Ser | |
| ENST00000682859.1:c.3935A>C | ENSP00000508222.1:p.Tyr1312Ser | |
| ENST00000683791.1:c.685+18552A>C | ||
| ENST00000684460.1:c.1387A>C | ||
| ENST00000684548.1:c.3935A>C | ENSP00000507421.1:p.Tyr1312Ser | |
| ENST00000684656.1:c.1387A>C | ||
| ENST00000613296.6:c.4316A>C MANE Select | ENSP00000482968.1:p.Tyr1439Ser | |
| ENST00000484298.5:c.4190A>C | ENSP00000478155.1:p.Tyr1397Ser | |
| ENST00000613296.4:c.4316A>C | ENSP00000482968.1:p.Tyr1439Ser | |
| ENST00000614410.4:c.4316A>C | ENSP00000479094.1:p.Tyr1439Ser | |
| NM_015120.4:c.4319A>C , LRG_741t1:c.4319A>C | NP_055935.4:p.Tyr1440Ser | |
| NM_001378454.1:c.4316A>C MANE Select | NP_001365383.1:p.Tyr1439Ser |