Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63086009G= , CM000670.2:g.63086009G= | GRCh38 |
| NC_000008.10:g.63998568G= , CM000670.1:g.63998568G= | GRCh37 |
| NC_000008.9:g.64161122G= | NCBI36 |
| NG_016123.1:g.5045C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000370.3:c.13C= MANE Select | NP_000361.1:p.Arg5= |
| ENST00000260116.5:c.13C= MANE Select | ENSP00000260116.4:p.Arg5= |
| ENST00000260116.4:c.13C= | ENSP00000260116.4:p.Arg5= |
| ENST00000521138.1:n.41C= | |
| XM_006716468.2:c.13C= | XP_006716531.1:p.Arg5= |
| XM_006716468.4:c.13C= | XP_006716531.1:p.Arg5= |