Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16993214T>A , CM000670.2:g.16993214T>A | GRCh38 |
| NC_000008.10:g.16850723T>A , CM000670.1:g.16850723T>A | GRCh37 |
| NC_000008.9:g.16895094T>A | NCBI36 |
| NG_015978.1:g.13952A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.494A>T MANE Select | ENSP00000180166.5:p.Tyr165Phe | |
| ENST00000180166.5:c.494A>T | ENSP00000180166.5:p.Tyr165Phe | |
| ENST00000519941.1:c.198A>T | ||
| NM_019851.2:c.494A>T | NP_062825.1:p.Tyr165Phe | |
| NM_019851.3:c.494A>T MANE Select | NP_062825.1:p.Tyr165Phe |