Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47744842C>A , CM000679.2:g.47744842C>A | GRCh38 |
| NC_000017.10:g.45822208C>A , CM000679.1:g.45822208C>A | GRCh37 |
| NC_000017.9:g.43177207C>A | NCBI36 |
| NG_012166.1:g.16599C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.1084C>A MANE Select | ENSP00000177694.1:p.Gln362Lys | |
| ENST00000177694.1:c.1084C>A | ENSP00000177694.1:p.Gln362Lys | |
| NM_013351.1:c.1084C>A | NP_037483.1:p.Gln362Lys | |
| XM_011524698.1:c.1147C>A | XP_011523000.1:p.Gln383Lys | |
| XM_011524699.1:c.751C>A | XP_011523001.1:p.Gln251Lys | |
| NM_013351.2:c.1084C>A MANE Select | NP_037483.1:p.Gln362Lys |