Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586533C= , CM000673.2:g.67586533C= | GRCh38 |
| NC_000011.9:g.67354004C= , CM000673.1:g.67354004C= | GRCh37 |
| NC_000011.8:g.67110580C= | NCBI36 |
| NG_012075.1:g.7939C= , LRG_723:g.7939C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.481C= | ENSP00000381604.1:p.Pro161= | |
| ENST00000398606.10:c.589C= MANE Select | ENSP00000381607.3:p.Pro197= | |
| ENST00000398603.5:c.481C= | ENSP00000381604.1:p.Pro161= | |
| ENST00000398606.7:c.589C= | ENSP00000381607.3:p.Pro197= | |
| ENST00000467591.1:n.700C= | ||
| ENST00000494593.1:n.1561C= | ||
| ENST00000498765.5:c.652C= | ||
| NM_000852.3:c.589C= , LRG_723t1:c.589C= | NP_000843.1:p.Pro197= | |
| NM_000852.4:c.589C= MANE Select | NP_000843.1:p.Pro197= |