Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111119042C>T , CM000667.2:g.111119042C>T | GRCh38 |
| NC_000005.9:g.110454740C>T , CM000667.1:g.110454740C>T | GRCh37 |
| NC_000005.8:g.110482639C>T | NCBI36 |
| NG_008979.1:g.31871C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513710.4:c.1826C>T MANE Select | ENSP00000424628.3:p.Ala609Val | |
| ENST00000506538.6:c.1994C>T | ENSP00000423067.2:p.Ala665Val | |
| ENST00000513710.3:c.1826C>T | ENSP00000424628.3:p.Ala609Val | |
| ENST00000612402.4:c.1994C>T | ENSP00000479950.1:p.Ala665Val | |
| NM_139281.2:c.1994C>T | NP_644810.1:p.Ala665Val | |
| XM_011543163.1:c.1994C>T | XP_011541465.1:p.Ala665Val | |
| NM_139281.3:c.1826C>T MANE Select | NP_644810.2:p.Ala609Val |