Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.147831617C= , CM000667.2:g.147831617C= | GRCh38 |
| NC_000005.9:g.147211180C= , CM000667.1:g.147211180C= | GRCh37 |
| NC_000005.8:g.147191373C= | NCBI36 |
| NG_008356.2:g.12615G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296695.10:c.-40G= MANE Select | ENSP00000296695.5:n.-40G= | |
| ENST00000296695.9:c.-40G= | ENSP00000296695.5:n.-40G= | |
| ENST00000510027.2:c.-40G= | ENSP00000427376.1:n.-40G= | |
| NM_003122.4:c.-40G= | NP_003113.2:n.-40G= | |
| NM_001354966.1:c.-40G= | NP_001341895.1:n.-40G= | |
| NM_001354966.2:c.-40G= | NP_001341895.1:n.-40G= | |
| NM_001379610.1:c.-40G= MANE Select | NP_001366539.1:n.-40G= | |
| NM_003122.5:c.-40G= | NP_003113.2:n.-40G= |