Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94408780G>T , CM000669.2:g.94408780G>T | GRCh38 |
| NC_000007.13:g.94038092G>T , CM000669.1:g.94038092G>T | GRCh37 |
| NC_000007.12:g.93876028G>T | NCBI36 |
| NG_007405.1:g.19220G>T , LRG_2:g.19220G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.749G>T MANE Select | NP_000080.2:p.Gly250Val |
| ENST00000297268.11:c.749G>T MANE Select | ENSP00000297268.6:p.Gly250Val |
| NM_000089.3:c.749G>T , LRG_2t1:c.749G>T | NP_000080.2:p.Gly250Val |
| ENST00000297268.10:c.749G>T | ENSP00000297268.6:p.Gly250Val |
| ENST00000620463.1:c.743G>T | ENSP00000477719.1:p.Gly248Val |