Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.83879731T= , CM000675.2:g.83879731T= | GRCh38 |
| NC_000013.10:g.84453866T= , CM000675.1:g.84453866T= | GRCh37 |
| NC_000013.9:g.83351867T= | NCBI36 |
| NG_016748.1:g.7663A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674365.1:c.1777A= MANE Select | ENSP00000501349.1:p.Ser593= | |
| ENST00000377084.3:c.1777A= | ENSP00000366288.2:p.Ser593= | |
| NM_001281503.1:c.1777A= | NP_001268432.1:p.Ser593= | |
| NM_052910.2:c.1777A= | NP_443142.1:p.Ser593= | |
| NM_001281503.2:c.1777A= MANE Select | NP_001268432.1:p.Ser593= |