Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111119021A= , CM000667.2:g.111119021A= | GRCh38 |
| NC_000005.9:g.110454719A= , CM000667.1:g.110454719A= | GRCh37 |
| NC_000005.8:g.110482618A= | NCBI36 |
| NG_008979.1:g.31850A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513710.4:c.1805A= MANE Select | ENSP00000424628.3:p.Asp602= | |
| ENST00000506538.6:c.1973A= | ENSP00000423067.2:p.Asp658= | |
| ENST00000513710.3:c.1805A= | ENSP00000424628.3:p.Asp602= | |
| ENST00000612402.4:c.1973A= | ENSP00000479950.1:p.Asp658= | |
| NM_139281.2:c.1973A= | NP_644810.1:p.Asp658= | |
| XM_011543163.1:c.1973A= | XP_011541465.1:p.Asp658= | |
| NM_139281.3:c.1805A= MANE Select | NP_644810.2:p.Asp602= |