Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107774871A>T , CM000669.2:g.107774871A>T | GRCh38 |
| NC_000007.13:g.107415316A>T , CM000669.1:g.107415316A>T | GRCh37 |
| NC_000007.12:g.107202552A>T | NCBI36 |
| NG_008046.1:g.33363T>A , LRG_683:g.33363T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000111.3:c.1679T>A MANE Select | NP_000102.1:p.Val560Asp |
| ENST00000340010.10:c.1679T>A MANE Select | ENSP00000345873.5:p.Val560Asp |
| NM_000111.2:c.1679T>A , LRG_683t1:c.1679T>A | NP_000102.1:p.Val560Asp |
| ENST00000340010.9:c.1679T>A | ENSP00000345873.5:p.Val560Asp |
| ENST00000379083.7:c.*1470T>A | ENSP00000368375.3:n.*1470T>A |
| XM_011515867.1:c.1679T>A | XP_011514169.1:p.Val560Asp |