Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12833688G>C , CM000686.2:g.12833688G>C | GRCh38 |
| NC_000024.9:g.14945614G>C , CM000686.1:g.14945614G>C | GRCh37 |
| NC_000024.8:g.13455008G>C | NCBI36 |
| NG_008311.1:g.137455G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651177.1:c.5022G>C | ENSP00000498372.1:p.Arg1674Ser | |
| ENST00000338981.7:c.5022G>C MANE Select | ENSP00000342812.3:p.Arg1674Ser | |
| ENST00000426564.6:n.5034G>C | ||
| NM_004654.3:c.5022G>C | NP_004645.2:p.Arg1674Ser | |
| XM_011531469.1:c.5022G>C | XP_011529771.1:p.Arg1674Ser | |
| XM_011531470.1:c.4788G>C | XP_011529772.1:p.Arg1596Ser | |
| XM_017030078.2:c.5037G>C | XP_016885567.1:p.Arg1679Ser | |
| NM_004654.4:c.5022G>C MANE Select | NP_004645.2:p.Arg1674Ser |