Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.96318482A= , CM000672.2:g.96318482A= | GRCh38 |
| NC_000010.10:g.98078239A= , CM000672.1:g.98078239A= | GRCh37 |
| NC_000010.9:g.98068229A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004088.4:c.334A= MANE Select | NP_004079.3:p.Arg112= |
| ENST00000371174.5:c.334A= MANE Select | ENSP00000360216.2:p.Arg112= |
| NM_001017520.1:c.334A= | NP_001017520.1:p.Arg112= |
| NM_001017520.2:c.334A= | NP_001017520.1:p.Arg112= |
| NM_004088.3:c.334A= | NP_004079.3:p.Arg112= |
| ENST00000371174.4:c.334A= | ENSP00000360216.2:p.Arg112= |
| ENST00000630152.1:c.334A= | ENSP00000486733.1:p.Arg112= |
| XM_011539420.1:c.334A= | XP_011537722.1:p.Arg112= |