Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67584733C>G , CM000673.2:g.67584733C>G | GRCh38 |
| NC_000011.9:g.67352204C>G , CM000673.1:g.67352204C>G | GRCh37 |
| NC_000011.8:g.67108780C>G | NCBI36 |
| NG_012075.1:g.6139C>G , LRG_723:g.6139C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.193C>G | ENSP00000381604.1:p.Gln65Glu | |
| ENST00000398606.10:c.193C>G MANE Select | ENSP00000381607.3:p.Gln65Glu | |
| ENST00000646888.1:c.86C>G | ENSP00000494477.1:p.Pro29Arg | |
| ENST00000398603.5:c.193C>G | ENSP00000381604.1:p.Gln65Glu | |
| ENST00000398606.7:c.193C>G | ENSP00000381607.3:p.Gln65Glu | |
| ENST00000489040.1:n.192C>G | ||
| ENST00000494593.1:n.623C>G | ||
| ENST00000498765.5:c.156C>G | ||
| NM_000852.3:c.193C>G , LRG_723t1:c.193C>G | NP_000843.1:p.Gln65Glu | |
| NM_000852.4:c.193C>G MANE Select | NP_000843.1:p.Gln65Glu |