Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44289685C= , CM000683.2:g.44289685C= | GRCh38 |
| NC_000021.8:g.45709568C= , CM000683.1:g.45709568C= | GRCh37 |
| NC_000021.7:g.44533996C= | NCBI36 |
| NG_009556.1:g.8806C= , LRG_18:g.8806C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000383.4:c.681C= MANE Select | NP_000374.1:p.Gly227= |
| ENST00000291582.6:c.681C= MANE Select | ENSP00000291582.5:p.Gly227= |
| NM_000383.3:c.681C= | NP_000374.1:p.Gly227= |
| ENST00000291582.5:c.681C= | ENSP00000291582.5:p.Gly227= |
| ENST00000527919.5:n.1414C= | |
| ENST00000530812.5:n.2431C= | |
| XM_011529551.1:c.681C= | XP_011527853.1:p.Gly227= |