Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44289789A= , CM000683.2:g.44289789A= | GRCh38 |
| NC_000021.8:g.45709672A= , CM000683.1:g.45709672A= | GRCh37 |
| NC_000021.7:g.44534100A= | NCBI36 |
| NG_009556.1:g.8910A= , LRG_18:g.8910A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.785A= MANE Select | ENSP00000291582.5:p.Gln262= | |
| ENST00000291582.5:c.785A= | ENSP00000291582.5:p.Gln262= | |
| ENST00000527919.5:n.1518A= | ||
| ENST00000530812.5:n.2535A= | ||
| NM_000383.3:c.785A= | NP_000374.1:p.Gln262= | |
| XM_011529551.1:c.785A= | XP_011527853.1:p.Gln262= | |
| NM_000383.4:c.785A= MANE Select | NP_000374.1:p.Gln262= |