Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.93218694A>G , CM000676.2:g.93218694A>G | GRCh38 |
| NC_000014.8:g.93685040A>G , CM000676.1:g.93685040A>G | GRCh37 |
| NC_000014.7:g.92754793A>G | NCBI36 |
| NG_051089.1:g.16639A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000013070.11:c.769A>G MANE Select | ENSP00000013070.6:p.Ser257Gly | |
| ENST00000013070.10:c.769A>G | ENSP00000013070.6:p.Ser257Gly | |
| ENST00000416753.5:c.541A>G | ENSP00000391706.2:p.Ser181Gly | |
| ENST00000553674.1:c.*470A>G | ENSP00000450470.1:n.*470A>G | |
| ENST00000553857.5:c.378+3413A>G | ||
| ENST00000555329.1:c.14A>G | ||
| NM_175748.3:c.769A>G | NP_786924.2:p.Ser257Gly | |
| NR_038150.1:n.871A>G | ||
| NM_175748.4:c.769A>G MANE Select | NP_786924.2:p.Ser257Gly | |
| NR_038150.2:n.671A>G |