Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129818869T>A , CM000671.2:g.129818869T>A | GRCh38 |
| NC_000009.11:g.132581148T>A , CM000671.1:g.132581148T>A | GRCh37 |
| NC_000009.10:g.131620969T>A | NCBI36 |
| NG_008049.1:g.10294A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.496A>T MANE Select | ENSP00000345719.4:p.Ile166Phe | |
| ENST00000651202.1:c.592A>T | ENSP00000498222.1:p.Ile198Phe | |
| ENST00000351698.4:c.496A>T | ENSP00000345719.4:p.Ile166Phe | |
| ENST00000473604.2:n.606A>T | ||
| NM_000113.2:c.496A>T | NP_000104.1:p.Ile166Phe | |
| XR_929731.1:n.656A>T | ||
| XR_929731.3:n.524A>T | ||
| NM_000113.3:c.496A>T MANE Select | NP_000104.1:p.Ile166Phe |