Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.55811875T= , CM000673.2:g.55811875T= | GRCh38 |
| NC_000011.9:g.55579351T= , CM000673.1:g.55579351T= | GRCh37 |
| NC_000011.8:g.55335927T= | NCBI36 |
| NG_052620.1:g.5509T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000625203.2:c.409T= MANE Select | ENSP00000485319.1:p.Ser137= | |
| ENST00000333973.3:c.409T= | ENSP00000335529.2:p.Ser137= | |
| ENST00000623450.1:c.409T= | ENSP00000485509.1:p.Ser137= | |
| ENST00000625203.1:c.409T= | ENSP00000485319.1:p.Ser137= | |
| NM_001004738.1:c.409T= | NP_001004738.1:p.Ser137= | |
| NM_001004738.2:c.409T= MANE Select | NP_001004738.1:p.Ser137= |