Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86629031G>A , CM000670.2:g.86629031G>A | GRCh38 |
| NC_000008.10:g.87641259G>A , CM000670.1:g.87641259G>A | GRCh37 |
| NC_000008.9:g.87710375G>A | NCBI36 |
| NG_016980.1:g.119645C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019098.5:c.1368C>T MANE Select | NP_061971.3:p.Arg456= |
| ENST00000320005.6:c.1368C>T MANE Select | ENSP00000316605.5:p.Arg456= |
| NM_019098.4:c.1368C>T | NP_061971.3:p.Arg456= |
| ENST00000320005.5:c.1368C>T | ENSP00000316605.5:p.Arg456= |
| ENST00000681546.1:n.1188C>T | |
| ENST00000681746.1:c.1368C>T | ENSP00000505959.1:p.Arg456= |
| XM_011517138.1:c.954C>T | XP_011515440.1:p.Arg318= |
| XM_011517138.2:c.954C>T | XP_011515440.1:p.Arg318= |