Linked Data
ClinVar Variation Id:
1610847
ClinVar RCV Id:
RCV002145576
dbSNP Id:
rs2110239545
MyVariant Identifiers:
chr4:g.100543987T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99622830T>G , CM000666.2:g.99622830T>G | GRCh38 |
| NC_000004.11:g.100543987T>G , CM000666.1:g.100543987T>G | GRCh37 |
| NC_000004.10:g.100763010T>G | NCBI36 |
| NG_011469.1:g.63748T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265517.10:c.2667T>G MANE Select | ENSP00000265517.5:p.Thr889= | |
| ENST00000457717.6:c.2667T>G | ENSP00000400821.1:p.Thr889= | |
| ENST00000511045.6:c.2418T>G | ENSP00000427679.2:p.Thr806= | |
| ENST00000265517.9:c.2667T>G | ENSP00000265517.5:p.Thr889= | |
| ENST00000457717.5:c.2667T>G | ENSP00000400821.1:p.Thr889= | |
| ENST00000511045.5:c.2748T>G | ENSP00000427679.1:p.Thr916= | |
| ENST00000619629.1:c.*1114T>G | ENSP00000482850.1:n.*1114T>G | |
| NM_000253.3:c.2667T>G | NP_000244.2:p.Thr889= | |
| NM_001300785.1:c.2748T>G | NP_001287714.1:p.Thr916= | |
| NM_000253.4:c.2667T>G | NP_000244.2:p.Thr889= | |
| NM_001300785.2:c.2418T>G | NP_001287714.2:p.Thr806= | |
| NM_001386140.1:c.2667T>G MANE Select | NP_001373069.1:p.Thr889= |