Linked Data
ClinVar Variation Id:
93803
dbSNP Id:
rs116343553
ExAC:
21:47410740 C / T
gnomAD v2:
21-47410740-C-T
gnomAD v3:
21-45990826-C-T
gnomAD v4:
21-45990826-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990826C>T , CM000683.2:g.45990826C>T | GRCh38 |
| NC_000021.8:g.47410740C>T , CM000683.1:g.47410740C>T | GRCh37 |
| NC_000021.7:g.46235168C>T | NCBI36 |
| NG_008674.1:g.14078C>T , LRG_475:g.14078C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361866.8:c.1056C>T MANE Select | ENSP00000355180.3:p.Asp352= | |
| ENST00000361866.7:c.1056C>T | ENSP00000355180.3:p.Asp352= | |
| ENST00000612273.1:c.1056C>T | ENSP00000483630.1:p.Asp352= | |
| NM_001848.2:c.1056C>T , LRG_475t1:c.1056C>T | NP_001839.2:p.Asp352= | |
| NM_001848.3:c.1056C>T MANE Select | NP_001839.2:p.Asp352= |