Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38252923G= , CM000677.2:g.38252923G= | GRCh38 |
| NC_000015.9:g.38545124G= , CM000677.1:g.38545124G= | GRCh37 |
| NC_000015.8:g.36332416G= | NCBI36 |
| NG_008980.1:g.5073G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.-263G= MANE Select | ENSP00000299084.4:n.-263G= | |
| ENST00000299084.8:c.-263G= | ENSP00000299084.4:n.-263G= | |
| ENST00000561205.1:n.76G= | ||
| NM_152594.2:c.-263G= | NP_689807.1:n.-263G= | |
| XM_005254202.2:c.-263G= | XP_005254259.1:n.-263G= | |
| XM_005254203.3:c.-310G= | XP_005254260.1:n.-310G= | |
| XM_005254202.3:c.-263G= | XP_005254259.1:n.-263G= | |
| XR_001751484.1:n.87+644C= | ||
| NM_152594.3:c.-263G= MANE Select | NP_689807.1:n.-263G= |