Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.6011283A>G , CM000672.2:g.6011283A>G | GRCh38 |
| NC_000010.10:g.6053246A>G , CM000672.1:g.6053246A>G | GRCh37 |
| NC_000010.9:g.6093252A>G | NCBI36 |
| NG_007403.1:g.56027T>C , LRG_73:g.56027T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379959.8:c.*1589T>C MANE Select | ENSP00000369293.3:n.*1589T>C | |
| ENST00000649218.1:n.2223T>C | ||
| ENST00000379959.7:c.*1589T>C | ENSP00000369293.3:n.*1589T>C | |
| NM_000417.2:c.*1589T>C , LRG_73t1:c.*1589T>C | NP_000408.1:n.*1589T>C | |
| NM_001308242.1:c.*1589T>C | NP_001295171.1:n.*1589T>C | |
| NM_001308243.1:c.*1589T>C | NP_001295172.1:n.*1589T>C | |
| NM_000417.3:c.*1589T>C MANE Select | NP_000408.1:n.*1589T>C | |
| NM_001308242.2:c.*1589T>C | NP_001295171.1:n.*1589T>C | |
| NM_001308243.2:c.*1589T>C | NP_001295172.1:n.*1589T>C |