Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94021651C>A , CM000663.2:g.94021651C>A | GRCh38 |
| NC_000001.10:g.94487207C>A , CM000663.1:g.94487207C>A | GRCh37 |
| NC_000001.9:g.94259795C>A | NCBI36 |
| NG_009073.1:g.104499G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4837G>T MANE Select | ENSP00000359245.3:p.Asp1613Tyr | |
| ENST00000370225.3:c.4837G>T | ENSP00000359245.3:p.Asp1613Tyr | |
| ENST00000460514.1:n.331G>T | ||
| ENST00000536513.5:c.1213G>T | ENSP00000439707.2:p.Asp405Tyr | |
| NM_000350.2:c.4837G>T | NP_000341.2:p.Asp1613Tyr | |
| NM_000350.3:c.4837G>T MANE Select | NP_000341.2:p.Asp1613Tyr |