Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229432123T>A , CM000663.2:g.229432123T>A | GRCh38 |
| NC_000001.10:g.229567870T>A , CM000663.1:g.229567870T>A | GRCh37 |
| NC_000001.9:g.227634493T>A | NCBI36 |
| NG_006672.1:g.6974A>T , LRG_429:g.6974A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.679A>T | ENSP00000355644.4:p.Asn227Tyr | |
| ENST00000684723.1:c.544A>T | ENSP00000508084.1:p.Asn182Tyr | |
| ENST00000366683.3:c.480-261A>T | ENSP00000355644.3:n.480-261A>T | |
| ENST00000366684.7:c.679A>T MANE Select | ENSP00000355645.3:p.Asn227Tyr | |
| NM_001100.3:c.679A>T , LRG_429t1:c.679A>T | NP_001091.1:p.Asn227Tyr | |
| NM_001100.4:c.679A>T MANE Select | NP_001091.1:p.Asn227Tyr |