Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47385211G= , CM000664.2:g.47385211G= | GRCh38 |
| NC_000002.11:g.47612350G= , CM000664.1:g.47612350G= | GRCh37 |
| NC_000002.10:g.47465854G= | NCBI36 |
| NG_012352.2:g.45049G= , LRG_215:g.45049G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002354.3:c.903+1G= MANE Select | NP_002345.2:n.903+1G= |
| ENST00000263735.9:c.903+1G= MANE Select | ENSP00000263735.4:n.903+1G= |
| NM_002354.2:c.903+1G= , LRG_215t1:c.903+1G= | NP_002345.2:n.903+1G= |
| ENST00000263735.8:c.903+1G= | ENSP00000263735.4:n.903+1G= |
| ENST00000405271.5:c.987+1G= | ENSP00000385476.1:n.987+1G= |
| ENST00000456133.5:c.987+1G= | ENSP00000410675.1:n.987+1G= |