Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536359G= , CM000679.2:g.42536359G= | GRCh38 |
| NC_000017.10:g.40688377G= , CM000679.1:g.40688377G= | GRCh37 |
| NC_000017.9:g.37941903G= | NCBI36 |
| NG_011552.1:g.5427G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.87G= MANE Select | ENSP00000225927.1:p.Ala29= | |
| ENST00000225927.6:c.87G= | ENSP00000225927.1:p.Ala29= | |
| NM_000263.3:c.87G= | NP_000254.2:p.Ala29= | |
| XM_024450771.1:c.87G= | XP_024306539.1:p.Ala29= | |
| NM_000263.4:c.87G= MANE Select | NP_000254.2:p.Ala29= |