Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48411042C>G , CM000677.2:g.48411042C>G | GRCh38 |
| NC_000015.9:g.48703239C>G , CM000677.1:g.48703239C>G | GRCh37 |
| NC_000015.8:g.46490531C>G | NCBI36 |
| NG_008805.2:g.239747G>C , LRG_778:g.239747G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1372G>C | ENSP00000453958.2:n.*1372G>C | |
| ENST00000682158.1:n.1945G>C | ||
| ENST00000682170.1:n.2745G>C | ||
| ENST00000682767.1:n.1861G>C | ||
| ENST00000316623.10:c.8564G>C MANE Select | ENSP00000325527.5:p.Ser2855Thr | |
| ENST00000316623.9:c.8564G>C | ENSP00000325527.5:p.Ser2855Thr | |
| ENST00000559133.5:c.3933G>C | ||
| NM_000138.4:c.8564G>C , LRG_778t1:c.8564G>C | NP_000129.3:p.Ser2855Thr | |
| NM_000138.5:c.8564G>C MANE Select | NP_000129.3:p.Ser2855Thr |