Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659387T>A , CM000685.2:g.136659387T>A | GRCh38 |
| NC_000023.10:g.135741546T>A , CM000685.1:g.135741546T>A | GRCh37 |
| NC_000023.9:g.135569212T>A | NCBI36 |
| NG_007280.1:g.16211T>A , LRG_141:g.16211T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*376T>A | ENSP00000512122.1:n.*376T>A | |
| ENST00000695725.1:c.*313T>A | ENSP00000512123.1:n.*313T>A | |
| ENST00000695726.1:n.2726T>A | ||
| ENST00000695729.1:n.3561T>A | ||
| ENST00000370629.7:c.758T>A MANE Select | ENSP00000359663.2:p.Phe253Tyr | |
| ENST00000370628.2:c.695T>A | ENSP00000359662.2:p.Phe232Tyr | |
| ENST00000370629.6:c.758T>A | ENSP00000359663.2:p.Phe253Tyr | |
| NM_000074.2:c.758T>A , LRG_141t1:c.758T>A | NP_000065.1:p.Phe253Tyr | |
| NM_000074.3:c.758T>A MANE Select | NP_000065.1:p.Phe253Tyr |