Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348587C>A , CM000685.2:g.101348587C>A | GRCh38 |
| NC_000023.10:g.100603575C>A , CM000685.1:g.100603575C>A | GRCh37 |
| NC_000023.9:g.100490231C>A | NCBI36 |
| NG_009616.1:g.42638G>T , LRG_128:g.42638G>T | |
| NG_011734.1:g.5383G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.4:c.78G>T MANE Select | ENSP00000361993.3:p.Glu26Asp | |
| ENST00000644112.2:c.78G>T | ENSP00000494385.1:p.Glu26Asp | |
| ENST00000645279.1:c.78G>T | ENSP00000494239.1:p.Glu26Asp | |
| ENST00000372902.3:c.78G>T | ENSP00000361993.3:p.Glu26Asp | |
| ENST00000480575.1:n.163G>T | ||
| NM_001145951.1:c.78G>T | NP_001139423.1:p.Glu26Asp | |
| NM_004085.3:c.78G>T | NP_004076.1:p.Glu26Asp | |
| NM_004085.4:c.78G>T MANE Select | NP_004076.1:p.Glu26Asp | |
| NM_001145951.2:c.78G>T | NP_001139423.1:p.Glu26Asp |