Linked Data
dbSNP Id:
rs758208915
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.64192311T>G , CM000685.2:g.64192311T>G | GRCh38 |
| NC_000023.10:g.63412191T>G , CM000685.1:g.63412191T>G | GRCh37 |
| NC_000023.9:g.63328916T>G | NCBI36 |
| NG_021345.1:g.18434A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374869.8:c.976A>C MANE Select | ENSP00000364003.4:p.Thr326Pro | |
| ENST00000330258.3:c.976A>C | ENSP00000329117.3:p.Thr326Pro | |
| ENST00000374869.7:c.976A>C | ENSP00000364003.3:p.Thr326Pro | |
| NM_152424.3:c.976A>C | NP_689637.3:p.Thr326Pro | |
| XM_011530858.1:c.976A>C | XP_011529160.1:p.Thr326Pro | |
| NM_152424.4:c.976A>C MANE Select | NP_689637.3:p.Thr326Pro |