Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12846348C>G , CM000686.2:g.12846348C>G | GRCh38 |
| NC_000024.9:g.14958273C>G , CM000686.1:g.14958273C>G | GRCh37 |
| NC_000024.8:g.13467667C>G | NCBI36 |
| NG_008311.1:g.150114C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651177.1:c.6584C>G | ENSP00000498372.1:p.Thr2195Arg | |
| ENST00000338981.7:c.6584C>G MANE Select | ENSP00000342812.3:p.Thr2195Arg | |
| ENST00000426564.6:n.6611C>G | ||
| NM_004654.3:c.6584C>G | NP_004645.2:p.Thr2195Arg | |
| XM_011531469.1:c.6584C>G | XP_011529771.1:p.Thr2195Arg | |
| XM_011531470.1:c.6350C>G | XP_011529772.1:p.Thr2117Arg | |
| XM_017030078.2:c.6599C>G | XP_016885567.1:p.Thr2200Arg | |
| NM_004654.4:c.6584C>G MANE Select | NP_004645.2:p.Thr2195Arg |