Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94949120T>G , CM000672.2:g.94949120T>G | GRCh38 |
| NC_000010.10:g.96708877T>G , CM000672.1:g.96708877T>G | GRCh37 |
| NC_000010.9:g.96698867T>G | NCBI36 |
| NG_008385.1:g.15463T>G | |
| NG_008385.2:g.15963T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.655T>G MANE Select | ENSP00000260682.6:p.Phe219Val | |
| ENST00000643112.1:c.655T>G | ENSP00000496202.1:p.Phe219Val | |
| ENST00000260682.6:c.655T>G | ENSP00000260682.6:p.Phe219Val | |
| ENST00000473496.1:n.426T>G | ||
| NM_000771.3:c.655T>G | NP_000762.2:p.Phe219Val | |
| NM_000771.4:c.655T>G MANE Select | NP_000762.2:p.Phe219Val |