Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.819754C>T , CM000673.2:g.819754C>T | GRCh38 |
| NC_000011.9:g.819754C>T , CM000673.1:g.819754C>T | GRCh37 |
| NC_000011.8:g.809754C>T | NCBI36 |
| NG_023394.1:g.5854C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020376.4:c.36C>T MANE Select | NP_065109.1:p.Phe12= |
| ENST00000336615.9:c.36C>T MANE Select | ENSP00000337701.4:p.Phe12= |
| NM_020376.3:c.36C>T | NP_065109.1:p.Phe12= |
| ENST00000336615.8:c.36C>T | ENSP00000337701.4:p.Phe12= |
| XM_006718265.2:c.36C>T | XP_006718328.1:p.Phe12= |
| XM_006718265.3:c.36C>T | XP_006718328.1:p.Phe12= |
| XM_006718266.2:c.36C>T | XP_006718329.1:p.Phe12= |
| XM_006718266.3:c.36C>T | XP_006718329.1:p.Phe12= |
| XM_017018028.1:c.36C>T | XP_016873517.1:p.Phe12= |
| XM_024448618.1:c.36C>T | XP_024304386.1:p.Phe12= |