Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945593C>G , CM000665.2:g.138945593C>G | GRCh38 |
| NC_000003.11:g.138664435C>G , CM000665.1:g.138664435C>G | GRCh37 |
| NC_000003.10:g.140147125C>G | NCBI36 |
| NG_012454.1:g.6548G>C | |
| NG_029796.1:g.3360C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.1130G>C MANE Select | ENSP00000497217.1:p.Ter377Ser | |
| ENST00000330315.3:c.1130G>C | ENSP00000333188.3:p.Ter377Ser | |
| NM_023067.3:c.1130G>C | NP_075555.1:p.Ter377Ser | |
| NM_023067.4:c.1130G>C MANE Select | NP_075555.1:p.Ter377Ser |