Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24205102T>A , CM000668.2:g.24205102T>A | GRCh38 |
| NC_000006.11:g.24205330T>A , CM000668.1:g.24205330T>A | GRCh37 |
| NC_000006.10:g.24313309T>A | NCBI36 |
| NG_012829.1:g.157951A>T | |
| NG_012829.2:g.183191A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.923A>T MANE Select | ENSP00000367715.3:p.Asp308Val | |
| ENST00000378450.6:c.182A>T | ENSP00000367711.3:p.Asp61Val | |
| ENST00000378454.7:c.923A>T | ENSP00000367715.3:p.Asp308Val | |
| NM_001195610.1:c.923A>T | NP_001182539.1:p.Asp308Val | |
| NM_016356.4:c.923A>T | NP_057440.2:p.Asp308Val | |
| NM_016356.5:c.923A>T MANE Select | NP_057440.2:p.Asp308Val | |
| NM_001195610.2:c.923A>T | NP_001182539.1:p.Asp308Val |