Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7445306A= , CM000679.2:g.7445306A= | GRCh38 |
| NC_000017.10:g.7348625A= , CM000679.1:g.7348625A= | GRCh37 |
| NC_000017.9:g.7289349A= | NCBI36 |
| NG_008026.1:g.5220A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000747.3:c.95A= MANE Select | NP_000738.2:p.Glu32= |
| ENST00000306071.7:c.95A= MANE Select | ENSP00000304290.2:p.Glu32= |
| NM_000747.2:c.95A= | NP_000738.2:p.Glu32= |
| ENST00000306071.6:c.95A= | ENSP00000304290.2:p.Glu32= |
| ENST00000572857.5:c.95A= | ENSP00000461402.1:p.Glu32= |
| ENST00000574054.1:n.115A= |