Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585212A= , CM000673.2:g.67585212A= | GRCh38 |
| NC_000011.9:g.67352683A= , CM000673.1:g.67352683A= | GRCh37 |
| NC_000011.8:g.67109259A= | NCBI36 |
| NG_012075.1:g.6618A= , LRG_723:g.6618A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.307A= | ENSP00000381604.1:p.Lys103= | |
| ENST00000398606.10:c.307A= MANE Select | ENSP00000381607.3:p.Lys103= | |
| ENST00000646888.1:c.*23A= | ENSP00000494477.1:n.*23A= | |
| ENST00000398603.5:c.307A= | ENSP00000381604.1:p.Lys103= | |
| ENST00000398606.7:c.307A= | ENSP00000381607.3:p.Lys103= | |
| ENST00000467591.1:n.418A= | ||
| ENST00000494593.1:n.1102A= | ||
| ENST00000498765.5:c.370A= | ||
| NM_000852.3:c.307A= , LRG_723t1:c.307A= | NP_000843.1:p.Lys103= | |
| NM_000852.4:c.307A= MANE Select | NP_000843.1:p.Lys103= |