Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965590A>C , CM000670.2:g.37965590A>C | GRCh38 |
| NC_000008.10:g.37823108A>C , CM000670.1:g.37823108A>C | GRCh37 |
| NC_000008.9:g.37942265A>C | NCBI36 |
| NG_011936.1:g.6077T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.880T>G MANE Select | NP_000016.1:p.Leu294Val |
| ENST00000345060.5:c.880T>G MANE Select | ENSP00000343782.3:p.Leu294Val |
| NM_000025.2:c.880T>G | NP_000016.1:p.Leu294Val |
| ENST00000345060.4:c.880T>G | ENSP00000343782.3:p.Leu294Val |
| ENST00000520341.1:n.155T>G | |
| ENST00000520341.2:n.1008T>G | |
| ENST00000614635.1:c.880T>G | ENSP00000480325.1:p.Leu294Val |
| ENST00000647937.1:c.364T>G | ENSP00000497740.1:p.Leu122Val |