Linked Data
ClinVar Variation Id:
290832
dbSNP Id:
rs373511343
ExAC:
21:47422539 G / T
gnomAD v2:
21-47422539-G-T
gnomAD v3:
21-46002625-G-T
gnomAD v4:
21-46002625-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46002625G>T , CM000683.2:g.46002625G>T | GRCh38 |
| NC_000021.8:g.47422539G>T , CM000683.1:g.47422539G>T | GRCh37 |
| NC_000021.7:g.46246967G>T | NCBI36 |
| NG_008674.1:g.25877G>T , LRG_475:g.25877G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463060.6:n.748G>T | ||
| ENST00000612273.2:c.475G>T | ||
| ENST00000682634.1:c.475G>T | ||
| ENST00000361866.8:c.2349G>T MANE Select | ENSP00000355180.3:p.Arg783= | |
| ENST00000361866.7:c.2349G>T | ENSP00000355180.3:p.Arg783= | |
| ENST00000463060.5:n.748G>T | ||
| ENST00000486023.1:n.137G>T | ||
| ENST00000498614.5:n.583G>T | ||
| ENST00000612273.1:c.2343G>T | ENSP00000483630.1:p.Arg781= | |
| NM_001848.2:c.2349G>T , LRG_475t1:c.2349G>T | NP_001839.2:p.Arg783= | |
| NM_001848.3:c.2349G>T MANE Select | NP_001839.2:p.Arg783= |