Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19939448G>C , CM000670.2:g.19939448G>C | GRCh38 |
| NC_000008.10:g.19796959G>C , CM000670.1:g.19796959G>C | GRCh37 |
| NC_000008.9:g.19841239G>C | NCBI36 |
| NG_008855.1:g.5378G>C | |
| NG_008855.2:g.42732G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.8G>C MANE Select | ENSP00000497642.1:p.Ser3Thr | |
| ENST00000311322.8:c.8G>C | ENSP00000309757.6:p.Ser3Thr | |
| ENST00000519773.1:c.8G>C | ENSP00000431028.1:p.Ser3Thr | |
| ENST00000520959.5:c.-140-8732G>C | ENSP00000428496.1:n.-140-8732G>C | |
| ENST00000521994.1:n.193G>C | ||
| ENST00000522701.5:c.8G>C | ENSP00000428557.1:p.Ser3Thr | |
| ENST00000523696.1:n.77G>C | ||
| ENST00000524029.5:c.8G>C | ENSP00000428237.1:p.Ser3Thr | |
| NM_000237.2:c.8G>C | NP_000228.1:p.Ser3Thr | |
| NM_000237.3:c.8G>C MANE Select | NP_000228.1:p.Ser3Thr |