Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816796A>C , CM000681.2:g.4816796A>C | GRCh38 |
| NC_000019.9:g.4816808A>C , CM000681.1:g.4816808A>C | GRCh37 |
| NC_000019.8:g.4767808A>C | NCBI36 |
| NG_031998.1:g.19947T>G , LRG_358:g.19947T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1582T>G MANE Select | ENSP00000248244.4:p.Phe528Val | |
| ENST00000248244.5:c.1582T>G | ENSP00000248244.4:p.Phe528Val | |
| ENST00000621756.1:c.1165T>G | ENSP00000479467.1:p.Phe389Val | |
| NM_182919.3:c.1582T>G , LRG_358t1:c.1582T>G | NP_891549.1:p.Phe528Val | |
| NM_001385678.1:c.1540T>G | NP_001372607.1:p.Phe514Val | |
| NM_001385679.1:c.1447T>G | NP_001372608.1:p.Phe483Val | |
| NM_001385680.1:c.940T>G | NP_001372609.1:p.Phe314Val | |
| NM_182919.4:c.1582T>G MANE Select | NP_891549.1:p.Phe528Val |