Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19961004T>C , CM000670.2:g.19961004T>C | GRCh38 |
| NC_000008.10:g.19818515T>C , CM000670.1:g.19818515T>C | GRCh37 |
| NC_000008.9:g.19862795T>C | NCBI36 |
| NG_008855.1:g.26934T>C | |
| NG_008855.2:g.64288T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.1243T>C MANE Select | ENSP00000497642.1:p.Phe415Leu | |
| ENST00000650478.1:c.183T>C | ENSP00000497560.1:n.183T>C | |
| ENST00000311322.8:c.1243T>C | ENSP00000309757.6:p.Phe415Leu | |
| NM_000237.2:c.1243T>C | NP_000228.1:p.Phe415Leu | |
| NM_000237.3:c.1243T>C MANE Select | NP_000228.1:p.Phe415Leu |