Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624076A>C , CM000679.2:g.41624076A>C | GRCh38 |
| NC_000017.10:g.39780328A>C , CM000679.1:g.39780328A>C | GRCh37 |
| NC_000017.9:g.37033854A>C | NCBI36 |
| NG_008625.1:g.5555T>G | |
| NG_009090.2:g.167637T>G , LRG_401:g.167637T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.432+2T>G MANE Select | ENSP00000308452.8:n.432+2T>G | |
| ENST00000311208.12:c.432+2T>G | ENSP00000308452.8:n.432+2T>G | |
| ENST00000463128.5:c.-184+2T>G | ENSP00000468672.1:n.-184+2T>G | |
| ENST00000491673.1:n.498+2T>G | ||
| ENST00000493253.5:n.219+2T>G | ||
| ENST00000540235.5:c.183+2T>G | ENSP00000441751.2:n.183+2T>G | |
| ENST00000577817.3:c.387+2T>G | ENSP00000467418.1:n.387+2T>G | |
| NM_000422.2:c.432+2T>G | NP_000413.1:n.432+2T>G | |
| NM_000422.3:c.432+2T>G MANE Select | NP_000413.1:n.432+2T>G |