Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.108561807G= , CM000668.2:g.108561807G= | GRCh38 |
| NC_000006.11:g.108883010G= , CM000668.1:g.108883010G= | GRCh37 |
| NC_000006.10:g.108989703G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000406360.2:c.599G= MANE Select | ENSP00000385824.1:p.Ser200= | |
| ENST00000343882.10:c.599G= | ENSP00000339527.6:p.Ser200= | |
| ENST00000406360.1:c.599G= | ENSP00000385824.1:p.Ser200= | |
| NM_001455.3:c.599G= | NP_001446.1:p.Ser200= | |
| NM_201559.2:c.599G= | NP_963853.1:p.Ser200= | |
| XM_005266867.3:c.-86G= | XP_005266924.1:n.-86G= | |
| XM_005266867.4:c.-86G= | XP_005266924.1:n.-86G= | |
| NM_001455.4:c.599G= MANE Select | NP_001446.1:p.Ser200= | |
| NM_201559.3:c.599G= | NP_963853.1:p.Ser200= |