Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320416T>A , CM000667.2:g.159320416T>A | GRCh38 |
| NC_000005.9:g.158747424T>A , CM000667.1:g.158747424T>A | GRCh37 |
| NC_000005.8:g.158680002T>A | NCBI36 |
| NG_009618.1:g.15058A>T , LRG_71:g.15058A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.-44A>T | ENSP00000512849.1:n.-44A>T | |
| ENST00000696751.1:c.*82A>T | ENSP00000512850.1:n.*82A>T | |
| ENST00000231228.3:c.587A>T MANE Select | ENSP00000231228.2:p.Asp196Val | |
| ENST00000231228.2:c.587A>T | ENSP00000231228.2:p.Asp196Val | |
| NM_002187.2:c.587A>T , LRG_71t1:c.587A>T | NP_002178.2:p.Asp196Val | |
| NM_002187.3:c.587A>T MANE Select | NP_002178.2:p.Asp196Val |