Linked Data
dbSNP Id:
rs1871909542
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33055145T>G , CM000675.2:g.33055145T>G | GRCh38 |
| NC_000013.10:g.33629282T>G , CM000675.1:g.33629282T>G | GRCh37 |
| NC_000013.9:g.32527282T>G | NCBI36 |
| NG_011485.1:g.43712T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380099.4:c.1429T>G MANE Select | ENSP00000369442.3:p.Phe477Val | |
| ENST00000380099.3:c.1429T>G | ENSP00000369442.3:p.Phe477Val | |
| ENST00000487852.1:n.1437T>G | ||
| NM_004795.3:c.1429T>G | NP_004786.2:p.Phe477Val | |
| XM_006719895.1:c.508T>G | XP_006719958.1:p.Phe170Val | |
| XM_006719895.2:c.508T>G | XP_006719958.1:p.Phe170Val | |
| NM_004795.4:c.1429T>G MANE Select | NP_004786.2:p.Phe477Val |