Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.41746040T>A , CM000666.2:g.41746040T>A | GRCh38 |
| NC_000004.11:g.41748057T>A , CM000666.1:g.41748057T>A | GRCh37 |
| NC_000004.10:g.41442814T>A | NCBI36 |
| NG_008243.1:g.7931A>T , LRG_513:g.7931A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003924.4:c.712A>T MANE Select | NP_003915.2:p.Lys238Ter |
| ENST00000226382.4:c.712A>T MANE Select | ENSP00000226382.2:p.Lys238Ter |
| NM_003924.3:c.712A>T , LRG_513t1:c.712A>T | NP_003915.2:p.Lys238Ter |
| ENST00000226382.3:c.712A>T | ENSP00000226382.2:p.Lys238Ter |
| ENST00000510424.2:n.533A>T |