Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94404849G>T , CM000669.2:g.94404849G>T | GRCh38 |
| NC_000007.13:g.94034161G>T , CM000669.1:g.94034161G>T | GRCh37 |
| NC_000007.12:g.93872097G>T | NCBI36 |
| NG_007405.1:g.15289G>T , LRG_2:g.15289G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.389G>T MANE Select | NP_000080.2:p.Gly130Val |
| ENST00000297268.11:c.389G>T MANE Select | ENSP00000297268.6:p.Gly130Val |
| NM_000089.3:c.389G>T , LRG_2t1:c.389G>T | NP_000080.2:p.Gly130Val |
| ENST00000297268.10:c.389G>T | ENSP00000297268.6:p.Gly130Val |
| ENST00000620463.1:c.383G>T | ENSP00000477719.1:p.Gly128Val |