Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585222C>A , CM000673.2:g.67585222C>A | GRCh38 |
| NC_000011.9:g.67352693C>A , CM000673.1:g.67352693C>A | GRCh37 |
| NC_000011.8:g.67109269C>A | NCBI36 |
| NG_012075.1:g.6628C>A , LRG_723:g.6628C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000398603.6:c.317C>A | ENSP00000381604.1:p.Ser106Tyr | |
| ENST00000398606.10:c.317C>A MANE Select | ENSP00000381607.3:p.Ser106Tyr | |
| ENST00000646888.1:c.*33C>A | ENSP00000494477.1:n.*33C>A | |
| ENST00000398603.5:c.317C>A | ENSP00000381604.1:p.Ser106Tyr | |
| ENST00000398606.7:c.317C>A | ENSP00000381607.3:p.Ser106Tyr | |
| ENST00000467591.1:n.428C>A | ||
| ENST00000494593.1:n.1112C>A | ||
| ENST00000498765.5:c.380C>A | ||
| NM_000852.3:c.317C>A , LRG_723t1:c.317C>A | NP_000843.1:p.Ser106Tyr | |
| NM_000852.4:c.317C>A MANE Select | NP_000843.1:p.Ser106Tyr |