Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.17376303C>G , CM000685.2:g.17376303C>G | GRCh38 |
| NC_000023.10:g.17394426C>G , CM000685.1:g.17394426C>G | GRCh37 |
| NC_000023.9:g.17304347C>G | NCBI36 |
| NG_011553.2:g.5884C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001291867.2:c.546C>G MANE Select | NP_001278796.1:p.Asp182Glu |
| ENST00000676302.1:c.546C>G MANE Select | ENSP00000502262.1:p.Asp182Glu |
| NM_001291867.1:c.546C>G | NP_001278796.1:p.Asp182Glu |
| NM_198270.3:c.546C>G | NP_938011.1:p.Asp182Glu |
| NM_198270.4:c.546C>G | NP_938011.1:p.Asp182Glu |
| ENST00000380060.7:c.546C>G | ENSP00000369400.3:p.Asp182Glu |