Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.100539782G= , CM000663.2:g.100539782G= | GRCh38 |
| NC_000001.10:g.101005338G= , CM000663.1:g.101005338G= | GRCh37 |
| NC_000001.9:g.100777926G= | NCBI36 |
| NG_053134.1:g.6611G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000315033.5:c.816G= MANE Select | ENSP00000314223.4:p.Leu272= | |
| ENST00000315033.4:c.816G= | ENSP00000314223.4:p.Leu272= | |
| NM_022049.2:c.816G= | NP_071332.2:p.Leu272= | |
| NM_022049.3:c.816G= MANE Select | NP_071332.2:p.Leu272= |