Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215817143C= , CM000663.2:g.215817143C= | GRCh38 |
| NC_000001.10:g.215990485C= , CM000663.1:g.215990485C= | GRCh37 |
| NC_000001.9:g.214057108C= | NCBI36 |
| NG_009497.1:g.611254G= | |
| NG_009497.2:g.611306G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.9424G= MANE Select | ENSP00000305941.3:p.Gly3142= | |
| ENST00000674083.1:c.9424G= | ENSP00000501296.1:p.Gly3142= | |
| ENST00000307340.7:c.9424G= | ENSP00000305941.3:p.Gly3142= | |
| NM_206933.2:c.9424G= | NP_996816.2:p.Gly3142= | |
| NM_206933.3:c.9424G= | NP_996816.2:p.Gly3142= | |
| NM_206933.4:c.9424G= MANE Select | NP_996816.3:p.Gly3142= |