Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48409179C= , CM000677.2:g.48409179C= | GRCh38 |
| NC_000015.9:g.48701376C= , CM000677.1:g.48701376C= | GRCh37 |
| NC_000015.8:g.46488668C= | NCBI36 |
| NG_008805.2:g.241610G= , LRG_778:g.241610G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682170.1:n.4608G= | ||
| ENST00000682767.1:n.3724G= | ||
| ENST00000316623.10:c.*1811G= MANE Select | ENSP00000325527.5:n.*1811G= | |
| ENST00000316623.9:c.*1811G= | ENSP00000325527.5:n.*1811G= | |
| NM_000138.4:c.*1811G= , LRG_778t1:c.*1811G= | NP_000129.3:n.*1811G= | |
| NM_000138.5:c.*1811G= MANE Select | NP_000129.3:n.*1811G= |