Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31271604T>A , CM000668.2:g.31271604T>A | GRCh38 |
| NC_000006.11:g.31239381T>A , CM000668.1:g.31239381T>A | GRCh37 |
| NC_000006.10:g.31347360T>A | NCBI36 |
| NG_029422.2:g.5528A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.338A>T MANE Select | ENSP00000365402.5:p.Glu113Val | |
| ENST00000376228.9:c.338A>T | ENSP00000365402.5:p.Glu113Val | |
| ENST00000376237.8:c.338A>T | ENSP00000365412.4:p.Glu113Val | |
| ENST00000383329.7:c.338A>T | ENSP00000372819.3:p.Glu113Val | |
| ENST00000415537.1:c.336A>T | ||
| ENST00000484378.1:n.357A>T | ||
| ENST00000487245.5:n.447A>T | ||
| ENST00000495835.1:n.527A>T | ||
| NM_002117.5:c.338A>T | NP_002108.4:p.Glu113Val | |
| NM_002117.6:c.338A>T MANE Select | NP_002108.4:p.Glu113Val |