Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.122077495T>A , CM000667.2:g.122077495T>A | GRCh38 |
| NC_000005.9:g.121413190T>A , CM000667.1:g.121413190T>A | GRCh37 |
| NC_000005.8:g.121441089T>A | NCBI36 |
| NG_008722.1:g.5866A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002317.7:c.491A>T MANE Select | NP_002308.2:p.Asp164Val |
| ENST00000231004.5:c.491A>T MANE Select | ENSP00000231004.4:p.Asp164Val |
| NM_002317.5:c.491A>T | NP_002308.2:p.Asp164Val |
| NM_002317.6:c.491A>T | NP_002308.2:p.Asp164Val |
| ENST00000231004.4:c.491A>T | ENSP00000231004.4:p.Asp164Val |
| ENST00000639739.2:c.491A>T | ENSP00000492324.2:p.Asp164Val |