Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94425627T>C , CM000669.2:g.94425627T>C | GRCh38 |
| NC_000007.13:g.94054939T>C , CM000669.1:g.94054939T>C | GRCh37 |
| NC_000007.12:g.93892875T>C | NCBI36 |
| NG_007405.1:g.36067T>C , LRG_2:g.36067T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.2799T>C MANE Select | NP_000080.2:p.Asp933= |
| ENST00000297268.11:c.2799T>C MANE Select | ENSP00000297268.6:p.Asp933= |
| NM_000089.3:c.2799T>C , LRG_2t1:c.2799T>C | NP_000080.2:p.Asp933= |
| ENST00000297268.10:c.2799T>C | ENSP00000297268.6:p.Asp933= |
| ENST00000469732.1:n.582T>C | |
| ENST00000478215.1:n.358T>C | |
| ENST00000481570.5:n.2772T>C | |
| ENST00000620463.1:c.2793T>C | ENSP00000477719.1:p.Asp931= |