Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44292303G= , CM000683.2:g.44292303G= | GRCh38 |
| NC_000021.8:g.45712186G= , CM000683.1:g.45712186G= | GRCh37 |
| NC_000021.7:g.44536614G= | NCBI36 |
| NG_009556.1:g.11424G= , LRG_18:g.11424G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.997G= MANE Select | ENSP00000291582.5:p.Gly333= | |
| ENST00000291582.5:c.997G= | ENSP00000291582.5:p.Gly333= | |
| ENST00000337909.5:n.458G= | ||
| ENST00000397994.8:n.458G= | ||
| ENST00000527919.5:n.1727G= | ||
| ENST00000530812.5:n.2744G= | ||
| NM_000383.3:c.997G= | NP_000374.1:p.Gly333= | |
| XM_011529551.1:c.994G= | XP_011527853.1:p.Gly332= | |
| NM_000383.4:c.997G= MANE Select | NP_000374.1:p.Gly333= |