Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42721859A= , CM000668.2:g.42721859A= | GRCh38 |
| NC_000006.11:g.42689597A= , CM000668.1:g.42689597A= | GRCh37 |
| NC_000006.10:g.42797575A= | NCBI36 |
| NG_009176.1:g.5762T= | |
| NG_009176.2:g.5762T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.476T= MANE Select | ENSP00000230381.5:p.Leu159= | |
| ENST00000230381.6:c.476T= | ENSP00000230381.5:p.Leu159= | |
| NM_000322.4:c.476T= | NP_000313.2:p.Leu159= | |
| XR_427834.2:n.1131T= | ||
| XR_926295.1:n.1131T= | ||
| XR_427834.4:n.1181T= | ||
| XR_926295.3:n.1181T= | ||
| NM_000322.5:c.476T= MANE Select | NP_000313.2:p.Leu159= |