Linked Data
dbSNP Id:
rs1186183517
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763708G>C , CM000674.2:g.57763708G>C | GRCh38 |
| NC_000012.11:g.58157491G>C , CM000674.1:g.58157491G>C | GRCh37 |
| NC_000012.10:g.56443758G>C | NCBI36 |
| NG_007076.1:g.8486C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000713544.1:c.1397C>G | ENSP00000518840.1:p.Thr466Ser | |
| ENST00000713545.1:c.*321C>G | ENSP00000518841.1:n.*321C>G | |
| ENST00000228606.9:c.1316C>G MANE Select | ENSP00000228606.4:p.Thr439Ser | |
| ENST00000228606.8:c.1316C>G | ENSP00000228606.4:p.Thr439Ser | |
| ENST00000547344.5:n.1455C>G | ||
| NM_000785.3:c.1316C>G | NP_000776.1:p.Thr439Ser | |
| NM_000785.4:c.1316C>G MANE Select | NP_000776.1:p.Thr439Ser |