Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951926C>T , CM000670.2:g.19951926C>T | GRCh38 |
| NC_000008.10:g.19809437C>T , CM000670.1:g.19809437C>T | GRCh37 |
| NC_000008.9:g.19853717C>T | NCBI36 |
| NG_008855.1:g.17856C>T | |
| NG_008855.2:g.55210C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.407C>T MANE Select | ENSP00000497642.1:p.Ala136Val | |
| ENST00000311322.8:c.407C>T | ENSP00000309757.6:p.Ala136Val | |
| ENST00000520959.5:c.179C>T | ENSP00000428496.1:p.Ala60Val | |
| NM_000237.2:c.407C>T | NP_000228.1:p.Ala136Val | |
| NM_000237.3:c.407C>T MANE Select | NP_000228.1:p.Ala136Val |