Linked Data
ClinVar Variation Id:
937677
dbSNP Id:
rs150443513
ExAC:
10:75842216 C / G
gnomAD v2:
10-75842216-C-G
gnomAD v3:
10-74082458-C-G
gnomAD v4:
10-74082458-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.74082458C>G , CM000672.2:g.74082458C>G | GRCh38 |
| NC_000010.10:g.75842216C>G , CM000672.1:g.75842216C>G | GRCh37 |
| NC_000010.9:g.75512222C>G | NCBI36 |
| NG_008868.1:g.89345C>G , LRG_383:g.89345C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000211998.10:c.788C>G MANE Select | ENSP00000211998.5:p.Thr263Ser | |
| ENST00000211998.8:c.788C>G | ENSP00000211998.4:p.Thr263Ser | |
| ENST00000372755.7:c.788C>G | ENSP00000361841.3:p.Thr263Ser | |
| ENST00000478896.2:n.332-18596C>G | ||
| ENST00000623461.3:n.3591C>G | ||
| ENST00000624354.3:c.*543C>G | ENSP00000485551.1:n.*543C>G | |
| NM_003373.3:c.788C>G | NP_003364.1:p.Thr263Ser | |
| NM_014000.2:c.788C>G , LRG_383t1:c.788C>G | NP_054706.1:p.Thr263Ser | |
| XM_005270142.1:c.791C>G | XP_005270199.1:p.Thr264Ser | |
| XM_005270143.1:c.791C>G | XP_005270200.1:p.Thr264Ser | |
| XR_001747501.1:n.90-4731G>C | ||
| NM_003373.4:c.788C>G | NP_003364.1:p.Thr263Ser | |
| NM_014000.3:c.788C>G MANE Select | NP_054706.1:p.Thr263Ser |