Linked Data
gnomAD v4:
17-47286316-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47286316A>T , CM000679.2:g.47286316A>T | GRCh38 |
| NC_000017.10:g.45363682A>T , CM000679.1:g.45363682A>T | GRCh37 |
| NC_000017.9:g.42718681A>T | NCBI36 |
| NG_008332.2:g.37475A>T , LRG_481:g.37475A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.671A>T | ENSP00000513002.1:p.Asp224Val | |
| ENST00000559488.7:c.671A>T MANE Select | ENSP00000452786.2:p.Asp224Val | |
| ENST00000559488.5:c.671A>T | ENSP00000452786.1:p.Asp224Val | |
| ENST00000560629.1:c.636A>T | ||
| ENST00000571680.1:c.671A>T | ENSP00000461626.1:p.Asp224Val | |
| NM_000212.2:c.671A>T , LRG_481t1:c.671A>T | NP_000203.2:p.Asp224Val | |
| NM_000212.3:c.671A>T MANE Select | NP_000203.2:p.Asp224Val |