Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624109T>G , CM000679.2:g.41624109T>G | GRCh38 |
| NC_000017.10:g.39780361T>G , CM000679.1:g.39780361T>G | GRCh37 |
| NC_000017.9:g.37033887T>G | NCBI36 |
| NG_008625.1:g.5522A>C | |
| NG_009090.2:g.167604A>C , LRG_401:g.167604A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.401A>C MANE Select | ENSP00000308452.8:p.Tyr134Ser | |
| ENST00000311208.12:c.401A>C | ENSP00000308452.8:p.Tyr134Ser | |
| ENST00000463128.5:c.-215A>C | ENSP00000468672.1:n.-215A>C | |
| ENST00000491673.1:n.467A>C | ||
| ENST00000493253.5:n.188A>C | ||
| ENST00000540235.5:c.152A>C | ENSP00000441751.2:p.Tyr51Ser | |
| ENST00000577817.3:c.356A>C | ENSP00000467418.1:p.Tyr119Ser | |
| NM_000422.2:c.401A>C | NP_000413.1:p.Tyr134Ser | |
| NM_000422.3:c.401A>C MANE Select | NP_000413.1:p.Tyr134Ser |