Linked Data
dbSNP Id:
rs778656352
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31125720T>G , CM000668.2:g.31125720T>G | GRCh38 |
| NC_000006.11:g.31093497T>G , CM000668.1:g.31093497T>G | GRCh37 |
| NC_000006.10:g.31201476T>G | NCBI36 |
| NG_021348.1:g.15890T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259881.10:c.-184T>G MANE Select | ENSP00000259881.9:n.-184T>G | |
| ENST00000259881.9:c.-184T>G | ENSP00000259881.9:n.-184T>G | |
| ENST00000479581.5:n.61+10829T>G | ||
| ENST00000548049.1:n.161T>G | ||
| ENST00000550838.1:n.59-19T>G | ||
| ENST00000552747.1:n.53+10829T>G | ||
| NM_014068.2:c.-184T>G | NP_054787.2:n.-184T>G | |
| NM_014068.3:c.-184T>G MANE Select | NP_054787.2:n.-184T>G |