Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67939963A>C , CM000678.2:g.67939963A>C | GRCh38 |
| NC_000016.9:g.67973866A>C , CM000678.1:g.67973866A>C | GRCh37 |
| NC_000016.8:g.66531367A>C | NCBI36 |
| NG_009778.1:g.9150T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.1264T>G MANE Select | ENSP00000264005.5:p.Tyr422Asp | |
| ENST00000264005.9:c.1264T>G | ENSP00000264005.5:p.Tyr422Asp | |
| ENST00000570369.5:c.267T>G | ||
| ENST00000573538.5:c.1002T>G | ENSP00000463220.1:n.1002T>G | |
| NM_000229.1:c.1264T>G | NP_000220.1:p.Tyr422Asp | |
| NM_000229.2:c.1264T>G MANE Select | NP_000220.1:p.Tyr422Asp |