Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64753931A= , CM000673.2:g.64753931A= | GRCh38 |
| NC_000011.9:g.64521403A= , CM000673.1:g.64521403A= | GRCh37 |
| NC_000011.8:g.64277979A= | NCBI36 |
| NG_013018.1:g.11785T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005609.4:c.1187T= MANE Select | NP_005600.1:p.Leu396= |
| ENST00000164139.4:c.1187T= MANE Select | ENSP00000164139.3:p.Leu396= |
| NM_001164716.1:c.923T= | NP_001158188.1:p.Leu308= |
| NM_005609.2:c.1187T= | NP_005600.1:p.Leu396= |
| NM_005609.3:c.1187T= | NP_005600.1:p.Leu396= |
| ENST00000164139.3:c.1187T= | ENSP00000164139.3:p.Leu396= |
| ENST00000377432.7:c.923T= | ENSP00000366650.3:p.Leu308= |
| ENST00000460413.1:n.264T= |