Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46726761G= , CM000673.2:g.46726761G= | GRCh38 |
| NC_000011.9:g.46748311G= , CM000673.1:g.46748311G= | GRCh37 |
| NC_000011.8:g.46704887G= | NCBI36 |
| NG_008953.1:g.12569G= , LRG_551:g.12569G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000506.5:c.1054G= MANE Select | NP_000497.1:p.Glu352= |
| ENST00000311907.10:c.1054G= MANE Select | ENSP00000308541.5:p.Glu352= |
| NM_000506.3:c.1054G= | NP_000497.1:p.Glu352= |
| NM_000506.4:c.1054G= , LRG_551t1:c.1054G= | NP_000497.1:p.Glu352= |
| NM_001311257.1:c.1006G= | NP_001298186.1:p.Glu336= |
| NM_001311257.2:c.1006G= | NP_001298186.1:p.Glu336= |
| ENST00000311907.9:c.1054G= | ENSP00000308541.5:p.Glu352= |
| ENST00000530231.5:c.1054G= | ENSP00000433907.1:p.Glu352= |
| XR_428840.2:n.1098G= | |
| XR_428840.4:n.1089G= |