Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110187261G>A , CM000675.2:g.110187261G>A | GRCh38 |
| NC_000013.10:g.110839608G>A , CM000675.1:g.110839608G>A | GRCh37 |
| NC_000013.9:g.109637609G>A | NCBI36 |
| NG_011544.2:g.124889C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001845.6:c.1605C>T MANE Select | NP_001836.3:p.Phe535= |
| ENST00000375820.10:c.1605C>T MANE Select | ENSP00000364979.4:p.Phe535= |
| NM_001845.5:c.1605C>T | NP_001836.3:p.Phe535= |
| ENST00000375820.8:c.1605C>T | ENSP00000364979.4:p.Phe535= |
| ENST00000649738.1:n.1735C>T | |
| XM_011521048.1:c.1413C>T | XP_011519350.1:p.Phe471= |
| XM_011521048.2:c.1413C>T | XP_011519350.1:p.Phe471= |