Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.66781020A= , CM000677.2:g.66781020A= | GRCh38 |
| NC_000015.9:g.67073358A= , CM000677.1:g.67073358A= | GRCh37 |
| NC_000015.8:g.64860412A= | NCBI36 |
| NG_012244.1:g.83685A= | |
| NG_012244.2:g.83685A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000288840.10:c.976A= MANE Select | ENSP00000288840.5:p.Thr326= | |
| ENST00000288840.9:c.976A= | ENSP00000288840.5:p.Thr326= | |
| ENST00000557916.5:c.1108A= | ENSP00000452955.1:n.1108A= | |
| ENST00000559931.5:c.280A= | ENSP00000453446.1:n.280A= | |
| NM_005585.4:c.976A= | NP_005576.3:p.Thr326= | |
| NR_027654.1:n.2031A= | ||
| XM_011521561.1:c.193A= | XP_011519863.1:p.Thr65= | |
| XR_931825.1:n.2375A= | ||
| XM_011521561.2:c.193A= | XP_011519863.1:p.Thr65= | |
| NM_005585.5:c.976A= MANE Select | NP_005576.3:p.Thr326= | |
| NR_027654.2:n.2131A= |