Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128344385C= , CM000667.2:g.128344385C= | GRCh38 |
| NC_000005.9:g.127680077C= , CM000667.1:g.127680077C= | GRCh37 |
| NC_000005.8:g.127707976C= | NCBI36 |
| NG_008750.1:g.198659G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001999.4:c.3343G= MANE Select | NP_001990.2:p.Asp1115= |
| ENST00000262464.9:c.3343G= MANE Select | ENSP00000262464.4:p.Asp1115= |
| NM_001999.3:c.3343G= | NP_001990.2:p.Asp1115= |
| ENST00000262464.8:c.3343G= | ENSP00000262464.4:p.Asp1115= |
| ENST00000508053.5:c.3343G= | ENSP00000424571.1:p.Asp1115= |
| ENST00000508989.5:c.3244G= | ENSP00000425596.1:p.Asp1082= |
| ENST00000619499.4:c.3340G= | ENSP00000482132.1:p.Asp1114= |
| XM_017009228.2:c.3190G= | XP_016864717.1:p.Asp1064= |