Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67740549G>C , CM000666.2:g.67740549G>C | GRCh38 |
| NC_000004.11:g.68606267G>C , CM000666.1:g.68606267G>C | GRCh37 |
| NC_000004.10:g.68288862G>C | NCBI36 |
| NG_009293.1:g.20538C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.918C>G MANE Select | ENSP00000226413.5:p.His306Gln | |
| ENST00000226413.4:c.918C>G | ENSP00000226413.4:p.His306Gln | |
| ENST00000420975.2:c.790C>G | ENSP00000397561.2:n.790C>G | |
| NM_000406.2:c.918C>G | NP_000397.1:p.His306Gln | |
| NM_001012763.1:c.*40C>G | NP_001012781.1:n.*40C>G | |
| NM_000406.3:c.918C>G MANE Select | NP_000397.1:p.His306Gln | |
| NM_001012763.2:c.*40C>G | NP_001012781.1:n.*40C>G |