Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.95247081T>G , CM000670.2:g.95247081T>G | GRCh38 |
| NC_000008.10:g.96259309T>G , CM000670.1:g.96259309T>G | GRCh37 |
| NC_000008.9:g.96328485T>G | NCBI36 |
| NG_032804.1:g.27154A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_177965.4:c.*536A>C MANE Select | NP_808880.1:n.*536A>C |
| ENST00000286688.6:c.*536A>C MANE Select | ENSP00000286688.5:n.*536A>C |
| NM_001363260.1:c.*536A>C | NP_001350189.1:n.*536A>C |
| NM_177965.3:c.*536A>C | NP_808880.1:n.*536A>C |
| ENST00000286688.5:c.*536A>C | ENSP00000286688.5:n.*536A>C |
| XM_005250799.2:c.*536A>C | XP_005250856.2:n.*536A>C |