Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47374177C= , CM000664.2:g.47374177C= | GRCh38 |
| NC_000002.11:g.47601316C= , CM000664.1:g.47601316C= | GRCh37 |
| NC_000002.10:g.47454820C= | NCBI36 |
| NG_012352.2:g.34015C= , LRG_215:g.34015C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002354.3:c.425+129C= MANE Select | NP_002345.2:n.425+129C= |
| ENST00000263735.9:c.425+129C= MANE Select | ENSP00000263735.4:n.425+129C= |
| NM_002354.2:c.425+129C= , LRG_215t1:c.425+129C= | NP_002345.2:n.425+129C= |
| ENST00000263735.8:c.425+129C= | ENSP00000263735.4:n.425+129C= |
| ENST00000405271.5:c.509+129C= | ENSP00000385476.1:n.509+129C= |
| ENST00000456133.5:c.509+129C= | ENSP00000410675.1:n.509+129C= |
| ENST00000474691.1:n.693+129C= | |
| ENST00000490733.1:n.274+129C= |