Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46739341G= , CM000673.2:g.46739341G= | GRCh38 |
| NC_000011.9:g.46760891G= , CM000673.1:g.46760891G= | GRCh37 |
| NC_000011.8:g.46717467G= | NCBI36 |
| NG_008953.1:g.25149G= , LRG_551:g.25149G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000506.5:c.1802G= MANE Select | NP_000497.1:p.Gly601= |
| ENST00000311907.10:c.1802G= MANE Select | ENSP00000308541.5:p.Gly601= |
| NM_000506.3:c.1802G= | NP_000497.1:p.Gly601= |
| NM_000506.4:c.1802G= , LRG_551t1:c.1802G= | NP_000497.1:p.Gly601= |
| NM_001311257.1:c.1754G= | NP_001298186.1:p.Gly585= |
| NM_001311257.2:c.1754G= | NP_001298186.1:p.Gly585= |
| ENST00000311907.9:c.1802G= | ENSP00000308541.5:p.Gly601= |
| ENST00000530231.5:c.1685G= | ENSP00000433907.1:p.Gly562= |
| XR_428840.2:n.1664G= | |
| XR_428840.4:n.1655G= |