Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64754817A>G , CM000673.2:g.64754817A>G | GRCh38 |
| NC_000011.9:g.64522289A>G , CM000673.1:g.64522289A>G | GRCh37 |
| NC_000011.8:g.64278865A>G | NCBI36 |
| NG_013018.1:g.10899T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005609.4:c.875T>C MANE Select | NP_005600.1:p.Leu292Pro |
| ENST00000164139.4:c.875T>C MANE Select | ENSP00000164139.3:p.Leu292Pro |
| NM_001164716.1:c.611T>C | NP_001158188.1:p.Leu204Pro |
| NM_005609.2:c.875T>C | NP_005600.1:p.Leu292Pro |
| NM_005609.3:c.875T>C | NP_005600.1:p.Leu292Pro |
| ENST00000164139.3:c.875T>C | ENSP00000164139.3:p.Leu292Pro |
| ENST00000377432.7:c.611T>C | ENSP00000366650.3:p.Leu204Pro |