Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370631G= , CM000683.2:g.34370631G= | GRCh38 |
| NC_000021.8:g.35742930G= , CM000683.1:g.35742930G= | GRCh37 |
| NC_000021.7:g.34664800G= | NCBI36 |
| NG_008804.1:g.11608G= , LRG_291:g.11608G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290310.4:c.153G= MANE Select | ENSP00000290310.2:p.Leu51= | |
| ENST00000290310.3:c.153G= | ENSP00000290310.2:p.Leu51= | |
| NM_172201.1:c.153G= , LRG_291t1:c.153G= | NP_751951.1:p.Leu51= | |
| XR_937683.1:n.690C= | ||
| XR_937684.1:n.690C= | ||
| XR_001755012.2:n.811C= | ||
| XR_001755013.2:n.690C= | ||
| XR_937683.2:n.690C= | ||
| NM_172201.2:c.153G= MANE Select | NP_751951.1:p.Leu51= |