Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94031792C>A , CM000663.2:g.94031792C>A | GRCh38 |
| NC_000001.10:g.94497348C>A , CM000663.1:g.94497348C>A | GRCh37 |
| NC_000001.9:g.94269936C>A | NCBI36 |
| NG_009073.1:g.94358G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4114G>T MANE Select | ENSP00000359245.3:p.Asp1372Tyr | |
| ENST00000370225.3:c.4114G>T | ENSP00000359245.3:p.Asp1372Tyr | |
| ENST00000536513.5:c.490G>T | ENSP00000439707.2:p.Asp164Tyr | |
| NM_000350.2:c.4114G>T | NP_000341.2:p.Asp1372Tyr | |
| NM_000350.3:c.4114G>T MANE Select | NP_000341.2:p.Asp1372Tyr |