Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160425128A>T , CM000663.2:g.160425128A>T | GRCh38 |
| NC_000001.10:g.160394918A>T , CM000663.1:g.160394918A>T | GRCh37 |
| NC_000001.9:g.158661542A>T | NCBI36 |
| NG_023420.1:g.29555A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696602.1:c.1460A>T | ENSP00000512747.1:p.Glu487Val | |
| ENST00000368061.3:c.1316A>T MANE Select | ENSP00000357040.2:p.Glu439Val | |
| ENST00000368061.2:c.1316A>T | ENSP00000357040.2:p.Glu439Val | |
| NM_020335.2:c.1316A>T | NP_065068.1:p.Glu439Val | |
| XM_005245357.1:c.1316A>T | XP_005245414.1:p.Glu439Val | |
| XM_011509804.1:c.1316A>T | XP_011508106.1:p.Glu439Val | |
| NM_020335.3:c.1316A>T MANE Select | NP_065068.1:p.Glu439Val |