Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154947782A>G , CM000685.2:g.154947782A>G | GRCh38 |
| NC_000023.10:g.154176057A>G , CM000685.1:g.154176057A>G | GRCh37 |
| NC_000023.9:g.153829251A>G | NCBI36 |
| NG_011403.1:g.79942T>C | |
| NG_011403.2:g.79942T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.2029T>C MANE Select | ENSP00000353393.4:p.Phe677Leu | |
| ENST00000647125.1:c.*1779+6110T>C | ENSP00000496062.1:n.*1779+6110T>C | |
| ENST00000360256.8:c.2029T>C | ENSP00000353393.4:p.Phe677Leu | |
| NM_000132.3:c.2029T>C | NP_000123.1:p.Phe677Leu | |
| XM_011531126.1:c.1924T>C | XP_011529428.1:p.Phe642Leu | |
| NM_000132.4:c.2029T>C MANE Select | NP_000123.1:p.Phe677Leu |