Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86668165T>A , CM000670.2:g.86668165T>A | GRCh38 |
| NC_000008.10:g.87680393T>A , CM000670.1:g.87680393T>A | GRCh37 |
| NC_000008.9:g.87749509T>A | NCBI36 |
| NG_016980.1:g.80511A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.497A>T MANE Select | ENSP00000316605.5:p.Lys166Met | |
| ENST00000680314.1:n.258A>T | ||
| ENST00000681746.1:c.497A>T | ENSP00000505959.1:p.Lys166Met | |
| ENST00000320005.5:c.497A>T | ENSP00000316605.5:p.Lys166Met | |
| NM_019098.4:c.497A>T | NP_061971.3:p.Lys166Met | |
| XM_011517138.1:c.83A>T | XP_011515440.1:p.Lys28Met | |
| XM_011517138.2:c.83A>T | XP_011515440.1:p.Lys28Met | |
| NM_019098.5:c.497A>T MANE Select | NP_061971.3:p.Lys166Met |