Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19955876T= , CM000670.2:g.19955876T= | GRCh38 |
| NC_000008.10:g.19813387T= , CM000670.1:g.19813387T= | GRCh37 |
| NC_000008.9:g.19857667T= | NCBI36 |
| NG_008855.1:g.21806T= | |
| NG_008855.2:g.59160T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000237.3:c.811T= MANE Select | NP_000228.1:p.Ser271= |
| ENST00000650287.1:c.811T= MANE Select | ENSP00000497642.1:p.Ser271= |
| NM_000237.2:c.811T= | NP_000228.1:p.Ser271= |
| ENST00000311322.8:c.811T= | ENSP00000309757.6:p.Ser271= |