Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.84840529A>C , CM000677.2:g.84840529A>C | GRCh38 |
| NC_000015.9:g.85383760A>C , CM000677.1:g.85383760A>C | GRCh37 |
| NC_000015.8:g.83184764A>C | NCBI36 |
| NG_054748.1:g.28899A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258888.6:c.1250A>C MANE Select | ENSP00000258888.6:p.Asp417Ala | |
| ENST00000258888.5:c.1856A>C | ENSP00000258888.5:p.Asp619Ala | |
| NM_020778.4:c.1856A>C | NP_065829.3:p.Asp619Ala | |
| NM_020778.5:c.1250A>C MANE Select | NP_065829.4:p.Asp417Ala |