Linked Data
dbSNP Id:
rs2127490987
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32222687C>G , CM000668.2:g.32222687C>G | GRCh38 |
| NC_000006.11:g.32190464C>G , CM000668.1:g.32190464C>G | GRCh37 |
| NC_000006.10:g.32298442C>G | NCBI36 |
| NG_028190.1:g.6381G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375023.3:c.275G>C MANE Select | ENSP00000364163.3:p.Ser92Thr | |
| ENST00000473562.1:n.404G>C | ||
| NM_004557.3:c.275G>C | NP_004548.3:p.Ser92Thr | |
| NR_134949.1:n.414G>C | ||
| NR_134950.1:n.414G>C | ||
| NM_004557.4:c.275G>C MANE Select | NP_004548.3:p.Ser92Thr | |
| NR_134949.2:n.414G>C | ||
| NR_134950.2:n.414G>C |