Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.147413461C= , CM000665.2:g.147413461C= | GRCh38 |
| NC_000003.11:g.147131248C= , CM000665.1:g.147131248C= | GRCh37 |
| NC_000003.10:g.148613938C= | NCBI36 |
| NG_015886.1:g.9068C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282928.5:c.1254C= MANE Select | ENSP00000282928.4:p.Thr418= | |
| ENST00000282928.4:c.1254C= | ENSP00000282928.4:p.Thr418= | |
| ENST00000472523.1:n.521+19519C= | ||
| ENST00000488404.5:c.320C= | ||
| NM_003412.3:c.1254C= | NP_003403.2:p.Thr418= | |
| NM_003412.4:c.1254C= MANE Select | NP_003403.2:p.Thr418= |