Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80275177C= , CM000672.2:g.80275177C= | GRCh38 |
| NC_000010.10:g.82034933C= , CM000672.1:g.82034933C= | GRCh37 |
| NC_000010.9:g.82024913C= | NCBI36 |
| NG_008083.1:g.19502G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000429.3:c.791G= MANE Select | NP_000420.1:p.Arg264= |
| ENST00000372213.8:c.791G= MANE Select | ENSP00000361287.3:p.Arg264= |
| NM_000429.2:c.791G= | NP_000420.1:p.Arg264= |
| ENST00000372213.7:c.791G= | ENSP00000361287.3:p.Arg264= |
| ENST00000480845.1:n.23G= | |
| ENST00000485270.5:n.303G= | |
| XM_005269842.3:c.791G= | XP_005269899.1:p.Arg264= |
| XM_005269843.3:c.668G= | XP_005269900.1:p.Arg223= |