Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63072980T= , CM000670.2:g.63072980T= | GRCh38 |
| NC_000008.10:g.63985539T= , CM000670.1:g.63985539T= | GRCh37 |
| NC_000008.9:g.64148093T= | NCBI36 |
| NG_016123.1:g.18074A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000370.3:c.313A= MANE Select | NP_000361.1:p.Arg105= |
| ENST00000260116.5:c.313A= MANE Select | ENSP00000260116.4:p.Arg105= |
| ENST00000260116.4:c.313A= | ENSP00000260116.4:p.Arg105= |
| ENST00000521138.1:n.232+12838A= | |
| XM_006716468.2:c.205-8664A= | XP_006716531.1:n.205-8664A= |
| XM_006716468.4:c.205-8664A= | XP_006716531.1:n.205-8664A= |