Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44290131T= , CM000683.2:g.44290131T= | GRCh38 |
| NC_000021.8:g.45710014T= , CM000683.1:g.45710014T= | GRCh37 |
| NC_000021.7:g.44534442T= | NCBI36 |
| NG_009556.1:g.9252T= , LRG_18:g.9252T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.879+63T= MANE Select | ENSP00000291582.5:n.879+63T= | |
| ENST00000291582.5:c.879+63T= | ENSP00000291582.5:n.879+63T= | |
| ENST00000527919.5:n.1612+63T= | ||
| ENST00000530812.5:n.2629+63T= | ||
| NM_000383.3:c.879+63T= | NP_000374.1:n.879+63T= | |
| XM_011529551.1:c.879+63T= | XP_011527853.1:n.879+63T= | |
| NM_000383.4:c.879+63T= MANE Select | NP_000374.1:n.879+63T= |