Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.121846918T>A , CM000674.2:g.121846918T>A | GRCh38 |
| NC_000012.11:g.122284824T>A , CM000674.1:g.122284824T>A | GRCh37 |
| NC_000012.10:g.120769207T>A | NCBI36 |
| NG_016461.1:g.46694A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289004.8:c.775A>T MANE Select | ENSP00000289004.4:p.Asn259Tyr | |
| ENST00000543163.5:c.658A>T | ENSP00000441677.1:p.Asn220Tyr | |
| NM_001171993.1:c.658A>T | NP_001165464.1:p.Asn220Tyr | |
| NM_002150.2:c.775A>T | NP_002141.1:p.Asn259Tyr | |
| NM_002150.3:c.775A>T MANE Select | NP_002141.2:p.Asn259Tyr | |
| NM_001171993.2:c.658A>T | NP_001165464.1:p.Asn220Tyr |