Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714418T>A , CM000681.2:g.6714418T>A | GRCh38 |
| NC_000019.9:g.6714429T>A , CM000681.1:g.6714429T>A | GRCh37 |
| NC_000019.8:g.6665429T>A | NCBI36 |
| NG_009557.1:g.11234A>T , LRG_27:g.11234A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.410A>T | ENSP00000512083.1:p.Asp137Val | |
| ENST00000245907.11:c.533A>T MANE Select | ENSP00000245907.4:p.Asp178Val | |
| ENST00000245907.10:c.533A>T | ENSP00000245907.4:p.Asp178Val | |
| NM_000064.3:c.533A>T | NP_000055.2:p.Asp178Val | |
| NM_000064.4:c.533A>T MANE Select | NP_000055.2:p.Asp178Val |