Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44383630C= , CM000679.2:g.44383630C= | GRCh38 |
| NC_000017.10:g.42460998C= , CM000679.1:g.42460998C= | GRCh37 |
| NC_000017.9:g.39816524C= | NCBI36 |
| NG_008331.1:g.10876G= , LRG_479:g.10876G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000419.5:c.1073G= MANE Select | NP_000410.2:p.Arg358= |
| ENST00000262407.6:c.1073G= MANE Select | ENSP00000262407.5:p.Arg358= |
| NM_000419.3:c.1073G= , LRG_479t1:c.1073G= | NP_000410.2:p.Arg358= |
| NM_000419.4:c.1073G= | NP_000410.2:p.Arg358= |
| ENST00000262407.5:c.1073G= | ENSP00000262407.5:p.Arg358= |
| ENST00000592226.5:n.313G= | |
| ENST00000648408.1:c.504G= | |
| XM_011524749.1:c.1073G= | XP_011523051.1:p.Arg358= |
| XM_011524750.1:c.1073G= | XP_011523052.1:p.Arg358= |