Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94941912G= , CM000672.2:g.94941912G= | GRCh38 |
| NC_000010.10:g.96701669G= , CM000672.1:g.96701669G= | GRCh37 |
| NC_000010.9:g.96691659G= | NCBI36 |
| NG_008385.1:g.8255G= | |
| NG_008385.2:g.8755G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.223G= MANE Select | ENSP00000260682.6:p.Val75= | |
| ENST00000643112.1:c.223G= | ENSP00000496202.1:p.Val75= | |
| ENST00000645207.1:n.376G= | ||
| ENST00000260682.6:c.223G= | ENSP00000260682.6:p.Val75= | |
| ENST00000461906.1:n.248G= | ||
| NM_000771.3:c.223G= | NP_000762.2:p.Val75= | |
| NM_000771.4:c.223G= MANE Select | NP_000762.2:p.Val75= |