Linked Data
MyVariant Identifiers:
chr17:g.41063443A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911426A>G , CM000679.2:g.42911426A>G | GRCh38 |
| NC_000017.10:g.41063443A>G , CM000679.1:g.41063443A>G | GRCh37 |
| NC_000017.9:g.38316969A>G | NCBI36 |
| NG_011808.1:g.15629A>G , LRG_147:g.15629A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.1074A>G MANE Select | ENSP00000253801.1:p.Ter358= | |
| ENST00000253801.6:c.1074A>G | ENSP00000253801.1:p.Ter358= | |
| ENST00000585489.1:c.*466A>G | ENSP00000466202.1:n.*466A>G | |
| NM_000151.3:c.1074A>G | NP_000142.2:p.Ter358= | |
| NM_001270397.1:c.*466A>G | NP_001257326.1:n.*466A>G | |
| NM_000151.4:c.1074A>G MANE Select | NP_000142.2:p.Ter358= | |
| NM_001270397.2:c.*466A>G | NP_001257326.1:n.*466A>G |