Linked Data
ClinVar Variation Id:
2845278
ClinVar RCV Id:
RCV003744477
MyVariant Identifiers:
chr11:g.118183511T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312796T>G , CM000673.2:g.118312796T>G | GRCh38 |
| NC_000011.9:g.118183511T>G , CM000673.1:g.118183511T>G | GRCh37 |
| NC_000011.8:g.117688721T>G | NCBI36 |
| NG_007383.1:g.13217T>G , LRG_38:g.13217T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.282T>G MANE Select | ENSP00000354566.4:p.Gly94= | |
| ENST00000361763.8:c.282T>G | ENSP00000354566.4:p.Gly94= | |
| ENST00000526146.5:n.828T>G | ||
| ENST00000528435.5:n.835T>G | ||
| ENST00000528600.1:c.264T>G | ENSP00000433975.1:p.Gly88= | |
| ENST00000529713.5:n.388T>G | ||
| ENST00000531913.1:n.653T>G | ||
| NM_000733.3:c.282T>G , LRG_38t1:c.282T>G | NP_000724.1:p.Gly94= | |
| NM_000733.4:c.282T>G MANE Select | NP_000724.1:p.Gly94= |