Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150992309A>G , CM000669.2:g.150992309A>G | GRCh38 |
| NC_000007.13:g.150689397A>G , CM000669.1:g.150689397A>G | GRCh37 |
| NC_000007.12:g.150320330A>G | NCBI36 |
| NG_011992.1:g.6251A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000603.5:c.-52+1009A>G MANE Select | NP_000594.2:n.-52+1009A>G |
| ENST00000297494.8:c.-52+1009A>G MANE Select | ENSP00000297494.3:n.-52+1009A>G |
| NM_000603.4:c.-52+1009A>G | NP_000594.2:n.-52+1009A>G |
| ENST00000297494.7:c.-52+1009A>G | ENSP00000297494.3:n.-52+1009A>G |
| ENST00000461406.5:c.-149+1009A>G | ENSP00000417143.1:n.-149+1009A>G |