Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189035119T>A , CM000664.2:g.189035119T>A | GRCh38 |
| NC_000002.11:g.189899845T>A , CM000664.1:g.189899845T>A | GRCh37 |
| NC_000002.10:g.189608090T>A | NCBI36 |
| NG_011799.1:g.149761A>T | |
| NG_011799.2:g.149761A>T | |
| NG_011799.3:g.195183A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.4150A>T MANE Select | ENSP00000364000.3:p.Ile1384Phe | |
| ENST00000374866.7:c.4150A>T | ENSP00000364000.3:p.Ile1384Phe | |
| ENST00000618828.1:c.2989A>T | ENSP00000482184.1:p.Ile997Phe | |
| NM_000393.3:c.4150A>T | NP_000384.2:p.Ile1384Phe | |
| XM_011510573.1:c.4012A>T | XP_011508875.1:p.Ile1338Phe | |
| NM_000393.4:c.4150A>T | NP_000384.2:p.Ile1384Phe | |
| XM_011510573.3:c.4012A>T | XP_011508875.1:p.Ile1338Phe | |
| NM_000393.5:c.4150A>T MANE Select | NP_000384.2:p.Ile1384Phe |