Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320459C>A , CM000667.2:g.159320459C>A | GRCh38 |
| NC_000005.9:g.158747467C>A , CM000667.1:g.158747467C>A | GRCh37 |
| NC_000005.8:g.158680045C>A | NCBI36 |
| NG_009618.1:g.15015G>T , LRG_71:g.15015G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696750.1:c.-87G>T | ENSP00000512849.1:n.-87G>T | |
| ENST00000696751.1:c.*39G>T | ENSP00000512850.1:n.*39G>T | |
| ENST00000231228.3:c.544G>T MANE Select | ENSP00000231228.2:p.Gly182Trp | |
| ENST00000231228.2:c.544G>T | ENSP00000231228.2:p.Gly182Trp | |
| NM_002187.2:c.544G>T , LRG_71t1:c.544G>T | NP_002178.2:p.Gly182Trp | |
| XR_001742945.1:n.10C>A | ||
| NM_002187.3:c.544G>T MANE Select | NP_002178.2:p.Gly182Trp |