Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.116277089C= , CM000674.2:g.116277089C= | GRCh38 |
| NC_000012.11:g.116714894C= , CM000674.1:g.116714894C= | GRCh37 |
| NC_000012.10:g.115199277C= | NCBI36 |
| NG_023366.1:g.5098G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_015335.5:c.43G= MANE Select | NP_056150.1:p.Glu15= |
| ENST00000281928.9:c.43G= MANE Select | ENSP00000281928.3:p.Glu15= |
| NM_015335.4:c.43G= | NP_056150.1:p.Glu15= |
| ENST00000281928.7:c.43G= | ENSP00000281928.3:p.Glu15= |
| ENST00000650226.1:c.43G= | ENSP00000496981.1:p.Glu15= |
| XM_011538080.1:c.43G= | XP_011536382.1:p.Glu15= |
| XM_011538080.2:c.43G= | XP_011536382.1:p.Glu15= |
| XM_011538081.1:c.43G= | XP_011536383.1:p.Glu15= |
| XM_011538081.2:c.43G= | XP_011536383.1:p.Glu15= |
| XM_017019090.1:c.43G= | XP_016874579.1:p.Glu15= |