Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147132489G= , CM000669.2:g.147132489G= | GRCh38 |
| NC_000007.13:g.146829581G= , CM000669.1:g.146829581G= | GRCh37 |
| NC_000007.12:g.146460514G= | NCBI36 |
| NG_007092.2:g.1021129G= | |
| NG_007092.3:g.1021489G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1328G= MANE Select | ENSP00000354778.3:p.Ser443= | |
| ENST00000636561.1:n.1231G= | ||
| ENST00000636870.1:n.1190G= | ||
| ENST00000637150.1:n.1257G= | ||
| ENST00000637694.1:n.1231G= | ||
| ENST00000637825.1:n.811G= | ||
| ENST00000638117.1:n.1231G= | ||
| ENST00000361727.7:c.1328G= | ENSP00000354778.3:p.Ser443= | |
| NM_014141.5:c.1328G= | NP_054860.1:p.Ser443= | |
| XM_017011950.2:c.1328G= | XP_016867439.1:p.Ser443= | |
| NM_014141.6:c.1328G= MANE Select | NP_054860.1:p.Ser443= |