Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193251438G>T , CM000663.2:g.193251438G>T | GRCh38 |
| NC_000001.10:g.193220568G>T , CM000663.1:g.193220568G>T | GRCh37 |
| NC_000001.9:g.191487191G>T | NCBI36 |
| NG_012691.1:g.134481G>T , LRG_507:g.134481G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.*726G>T MANE Select | ENSP00000356405.4:n.*726G>T | |
| ENST00000635846.1:c.*726G>T | ENSP00000490035.1:n.*726G>T | |
| ENST00000643006.1:c.*1232G>T | ENSP00000496633.1:n.*1232G>T | |
| ENST00000367435.3:c.*726G>T | ENSP00000356405.3:n.*726G>T | |
| NM_024529.4:c.*726G>T , LRG_507t1:c.*726G>T | NP_078805.3:n.*726G>T | |
| NM_024529.5:c.*726G>T MANE Select | NP_078805.3:n.*726G>T |