Linked Data
ClinVar Variation Id:
2659061
ClinVar RCV Id:
RCV003425604
MyVariant Identifiers:
chr9:g.6556192T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6556192T>G , CM000671.2:g.6556192T>G | GRCh38 |
| NC_000009.11:g.6556192T>G , CM000671.1:g.6556192T>G | GRCh37 |
| NC_000009.10:g.6546192T>G | NCBI36 |
| NG_016397.1:g.94501A>C , LRG_643:g.94501A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000321612.8:c.2163A>C MANE Select | ENSP00000370737.4:p.Gly721= | |
| ENST00000638233.1:n.598A>C | ||
| ENST00000638661.1:c.363A>C | ENSP00000491369.1:p.Gly121= | |
| ENST00000638694.1:n.350A>C | ||
| ENST00000639318.1:c.363A>C | ENSP00000491932.1:p.Gly121= | |
| ENST00000639364.1:n.1863A>C | ||
| ENST00000639443.1:n.1731A>C | ||
| ENST00000639954.1:n.1871A>C | ||
| ENST00000640505.1:n.402A>C | ||
| ENST00000321612.6:c.2163A>C | ENSP00000370737.3:p.Gly721= | |
| NM_000170.2:c.2163A>C , LRG_643t1:c.2163A>C | NP_000161.2:p.Gly721= | |
| NM_000170.3:c.2163A>C MANE Select | NP_000161.2:p.Gly721= |