Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153695170G>T , CM000685.2:g.153695170G>T | GRCh38 |
| NC_000023.10:g.152960625G>T , CM000685.1:g.152960625G>T | GRCh37 |
| NC_000023.9:g.152613819G>T | NCBI36 |
| NG_012016.1:g.11874G>T | |
| NG_012016.2:g.11874G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005629.4:c.1864G>T MANE Select | NP_005620.1:p.Val622Leu |
| ENST00000253122.10:c.1864G>T MANE Select | ENSP00000253122.5:p.Val622Leu |
| NM_001142805.1:c.1834G>T | NP_001136277.1:p.Val612Leu |
| NM_001142805.2:c.1834G>T | NP_001136277.1:p.Val612Leu |
| NM_001142806.1:c.1519G>T | NP_001136278.1:p.Val507Leu |
| NM_005629.3:c.1864G>T | NP_005620.1:p.Val622Leu |
| ENST00000253122.9:c.1864G>T | ENSP00000253122.5:p.Val622Leu |
| ENST00000430077.6:c.1519G>T | ENSP00000403041.2:p.Val507Leu |
| ENST00000485324.1:n.2171G>T |