Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94406278G>T , CM000669.2:g.94406278G>T | GRCh38 |
| NC_000007.13:g.94035590G>T , CM000669.1:g.94035590G>T | GRCh37 |
| NC_000007.12:g.93873526G>T | NCBI36 |
| NG_007405.1:g.16718G>T , LRG_2:g.16718G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.569G>T MANE Select | NP_000080.2:p.Gly190Val |
| ENST00000297268.11:c.569G>T MANE Select | ENSP00000297268.6:p.Gly190Val |
| NM_000089.3:c.569G>T , LRG_2t1:c.569G>T | NP_000080.2:p.Gly190Val |
| ENST00000297268.10:c.569G>T | ENSP00000297268.6:p.Gly190Val |
| ENST00000620463.1:c.563G>T | ENSP00000477719.1:p.Gly188Val |