Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155133751A= , CM000663.2:g.155133751A= | GRCh38 |
| NC_000001.10:g.155106227A= , CM000663.1:g.155106227A= | GRCh37 |
| NC_000001.9:g.153372851A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368407.8:c.476A= MANE Select | ENSP00000357392.3:p.Asp159= | |
| ENST00000368406.2:c.410A= | ENSP00000357391.2:p.Asp137= | |
| ENST00000368407.7:c.476A= | ENSP00000357392.3:p.Asp159= | |
| ENST00000469878.5:n.727A= | ||
| ENST00000474413.5:n.701A= | ||
| ENST00000497282.1:n.519A= | ||
| NM_004428.2:c.476A= | NP_004419.2:p.Asp159= | |
| NM_182685.1:c.410A= | NP_872626.1:p.Asp137= | |
| XM_005244940.3:c.287A= | XP_005244997.1:p.Asp96= | |
| NM_004428.3:c.476A= MANE Select | NP_004419.2:p.Asp159= | |
| NM_182685.2:c.410A= | NP_872626.1:p.Asp137= |