Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117479282C= , CM000669.2:g.117479282C= | GRCh38 |
| NC_000007.13:g.117119336C= , CM000669.1:g.117119336C= | GRCh37 |
| NC_000007.12:g.116906572C= | NCBI36 |
| NG_016465.4:g.18499C= , LRG_663:g.18499C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000446805.2:c.-487C= | ENSP00000417012.1:n.-487C= | |
| ENST00000673785.1:c.-406+13451C= | ENSP00000501235.1:n.-406+13451C= | |
| ENST00000546407.1:n.166+3474C= | ||
| XM_011515751.1:c.80C= | XP_011514053.1:p.Thr27= | |
| XM_011515752.1:c.80C= | XP_011514054.1:p.Thr27= | |
| XM_011515754.1:c.-815C= | XP_011514056.1:n.-815C= |