Linked Data
ClinVar Variation Id:
2174090
ClinVar RCV Id:
RCV002584968
MyVariant Identifiers:
chr16:g.81391442A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81357837A>G , CM000678.2:g.81357837A>G | GRCh38 |
| NC_000016.9:g.81391442A>G , CM000678.1:g.81391442A>G | GRCh37 |
| NC_000016.8:g.79948943A>G | NCBI36 |
| NG_009007.1:g.47872A>G , LRG_242:g.47872A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*587A>G | ENSP00000498114.1:n.*587A>G | |
| ENST00000648994.2:c.879A>G MANE Select | ENSP00000497351.1:p.Arg293= | |
| ENST00000650388.1:c.413A>G | ENSP00000498081.1:n.413A>G | |
| ENST00000568107.2:c.879A>G | ENSP00000476795.1:p.Arg293= | |
| NM_022041.3:c.879A>G , LRG_242t1:c.879A>G | NP_071324.1:p.Arg293= | |
| XM_017023734.1:c.240A>G | XP_016879223.1:p.Arg80= | |
| NM_001377486.1:c.240A>G | NP_001364415.1:p.Arg80= | |
| NM_022041.4:c.879A>G MANE Select | NP_071324.1:p.Arg293= |