Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625325C= , CM000673.2:g.22625325C= | GRCh38 |
| NC_000011.9:g.22646871C= , CM000673.1:g.22646871C= | GRCh37 |
| NC_000011.8:g.22603447C= | NCBI36 |
| NG_007425.1:g.5517G= , LRG_527:g.5517G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.486G= MANE Select | ENSP00000330875.3:p.Leu162= | |
| ENST00000327470.4:c.486G= | ENSP00000330875.3:p.Leu162= | |
| NM_022725.3:c.486G= , LRG_527t1:c.486G= | NP_073562.1:p.Leu162= | |
| NM_022725.4:c.486G= MANE Select | NP_073562.1:p.Leu162= |