Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.24460652G= , CM000680.2:g.24460652G= | GRCh38 |
| NC_000018.9:g.22040616G= , CM000680.1:g.22040616G= | GRCh37 |
| NC_000018.8:g.20294614G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256906.5:c.-77G= MANE Select | ENSP00000256906.4:n.-77G= | |
| ENST00000256906.4:c.-77G= | ENSP00000256906.4:n.-77G= | |
| NM_001143828.1:c.-77G= | NP_001137300.1:n.-77G= | |
| NM_001160166.1:c.-77G= | NP_001153638.1:n.-77G= | |
| NM_021624.3:c.-77G= | NP_067637.2:n.-77G= | |
| XM_011526133.1:c.-77G= | XP_011524435.1:n.-77G= | |
| XM_011526134.1:c.-77G= | XP_011524436.1:n.-77G= | |
| NM_021624.4:c.-77G= MANE Select | NP_067637.2:n.-77G= | |
| NM_001143828.2:c.-77G= | NP_001137300.1:n.-77G= | |
| NM_001160166.2:c.-77G= | NP_001153638.1:n.-77G= |