Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94425136G>T , CM000669.2:g.94425136G>T | GRCh38 |
| NC_000007.13:g.94054448G>T , CM000669.1:g.94054448G>T | GRCh37 |
| NC_000007.12:g.93892384G>T | NCBI36 |
| NG_007405.1:g.35576G>T , LRG_2:g.35576G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.2693G>T MANE Select | ENSP00000297268.6:p.Gly898Val | |
| ENST00000297268.10:c.2693G>T | ENSP00000297268.6:p.Gly898Val | |
| ENST00000469732.1:n.476G>T | ||
| ENST00000481570.5:n.2666G>T | ||
| ENST00000620463.1:c.2687G>T | ENSP00000477719.1:p.Gly896Val | |
| NM_000089.3:c.2693G>T , LRG_2t1:c.2693G>T | NP_000080.2:p.Gly898Val | |
| NM_000089.4:c.2693G>T MANE Select | NP_000080.2:p.Gly898Val |