Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115705212C= , CM000663.2:g.115705212C= | GRCh38 |
| NC_000001.10:g.116247833C= , CM000663.1:g.116247833C= | GRCh37 |
| NC_000001.9:g.116049356C= | NCBI36 |
| NG_008802.1:g.68594G= , LRG_404:g.68594G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001232.4:c.919G= MANE Select | NP_001223.2:p.Asp307= |
| ENST00000261448.6:c.919G= MANE Select | ENSP00000261448.5:p.Asp307= |
| NM_001232.3:c.919G= , LRG_404t1:c.919G= | NP_001223.2:p.Asp307= |
| ENST00000261448.5:c.919G= | ENSP00000261448.5:p.Asp307= |
| ENST00000488931.2:c.*291G= | ENSP00000518226.1:n.*291G= |