Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586519C>G , CM000673.2:g.67586519C>G | GRCh38 |
| NC_000011.9:g.67353990C>G , CM000673.1:g.67353990C>G | GRCh37 |
| NC_000011.8:g.67110566C>G | NCBI36 |
| NG_012075.1:g.7925C>G , LRG_723:g.7925C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.467C>G | ENSP00000381604.1:p.Ala156Gly | |
| ENST00000398606.10:c.575C>G MANE Select | ENSP00000381607.3:p.Ala192Gly | |
| ENST00000398603.5:c.467C>G | ENSP00000381604.1:p.Ala156Gly | |
| ENST00000398606.7:c.575C>G | ENSP00000381607.3:p.Ala192Gly | |
| ENST00000467591.1:n.686C>G | ||
| ENST00000494593.1:n.1547C>G | ||
| ENST00000498765.5:c.638C>G | ||
| NM_000852.3:c.575C>G , LRG_723t1:c.575C>G | NP_000843.1:p.Ala192Gly | |
| NM_000852.4:c.575C>G MANE Select | NP_000843.1:p.Ala192Gly |