Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.105150705C= , CM000676.2:g.105150705C= | GRCh38 |
| NC_000014.8:g.105617042C= , CM000676.1:g.105617042C= | GRCh37 |
| NC_000014.7:g.104688087C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002226.5:c.1501G= MANE Select | NP_002217.3:p.Glu501= |
| ENST00000331782.8:c.1501G= MANE Select | ENSP00000328169.3:p.Glu501= |
| NM_002226.4:c.1501G= | NP_002217.3:p.Glu501= |
| NM_145159.2:c.1387G= | NP_660142.1:p.Glu463= |
| NM_145159.3:c.1387G= | NP_660142.1:p.Glu463= |
| ENST00000331782.7:c.1501G= | ENSP00000328169.3:p.Glu501= |
| ENST00000347004.2:c.1387G= | ENSP00000328566.2:p.Glu463= |
| XM_011536736.1:c.1501G= | XP_011535038.1:p.Glu501= |
| XR_001750303.2:n.1562G= |