Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045775G>A , CM000675.2:g.48045775G>A | GRCh38 |
| NC_000013.10:g.48619911G>A , CM000675.1:g.48619911G>A | GRCh37 |
| NC_000013.9:g.47517912G>A | NCBI36 |
| NG_047021.1:g.13209G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258662.3:c.471G>A MANE Select | ENSP00000258662.1:p.Val157= | |
| ENST00000258662.2:c.471G>A | ENSP00000258662.1:p.Val157= | |
| NM_018283.2:c.471G>A | NP_060753.1:p.Val157= | |
| NM_018283.3:c.471G>A | NP_060753.1:p.Val157= | |
| NR_136687.1:n.651G>A | ||
| NR_136688.1:n.651G>A | ||
| NM_018283.4:c.471G>A MANE Select | NP_060753.1:p.Val157= | |
| NR_136687.2:n.492G>A | ||
| NR_136688.2:n.492G>A |