Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33438912T= , CM000682.2:g.33438912T= | GRCh38 |
| NC_000020.10:g.32026718T= , CM000682.1:g.32026718T= | GRCh37 |
| NC_000020.9:g.31490379T= | NCBI36 |
| NG_011622.1:g.9981A= , LRG_332:g.9981A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.425A= MANE Select | ENSP00000217381.2:p.Asp142= | |
| ENST00000217381.2:c.425A= | ENSP00000217381.2:p.Asp142= | |
| NM_003098.2:c.425A= , LRG_332t1:c.425A= | NP_003089.1:p.Asp142= | |
| XM_005260517.1:c.425A= | XP_005260574.1:p.Asp142= | |
| XM_011529007.1:c.425A= | XP_011527309.1:p.Asp142= | |
| XM_011529008.1:c.425A= | XP_011527310.1:p.Asp142= | |
| XR_936612.1:n.658A= | ||
| XM_024451971.1:c.98A= | XP_024307739.1:p.Asp33= | |
| NM_003098.3:c.425A= MANE Select | NP_003089.1:p.Asp142= |