Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624107A>C , CM000679.2:g.41624107A>C | GRCh38 |
| NC_000017.10:g.39780359A>C , CM000679.1:g.39780359A>C | GRCh37 |
| NC_000017.9:g.37033885A>C | NCBI36 |
| NG_008625.1:g.5524T>G | |
| NG_009090.2:g.167606T>G , LRG_401:g.167606T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.403T>G MANE Select | ENSP00000308452.8:p.Tyr135Asp | |
| ENST00000311208.12:c.403T>G | ENSP00000308452.8:p.Tyr135Asp | |
| ENST00000463128.5:c.-213T>G | ENSP00000468672.1:n.-213T>G | |
| ENST00000491673.1:n.469T>G | ||
| ENST00000493253.5:n.190T>G | ||
| ENST00000540235.5:c.154T>G | ENSP00000441751.2:p.Tyr52Asp | |
| ENST00000577817.3:c.358T>G | ENSP00000467418.1:p.Tyr120Asp | |
| NM_000422.2:c.403T>G | NP_000413.1:p.Tyr135Asp | |
| NM_000422.3:c.403T>G MANE Select | NP_000413.1:p.Tyr135Asp |