Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159316780C= , CM000667.2:g.159316780C= | GRCh38 |
| NC_000005.9:g.158743788C= , CM000667.1:g.158743788C= | GRCh37 |
| NC_000005.8:g.158676366C= | NCBI36 |
| NG_009618.1:g.18694G= , LRG_71:g.18694G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.262G= | ENSP00000512849.1:p.Val88= | |
| ENST00000696751.1:c.*387G= | ENSP00000512850.1:n.*387G= | |
| ENST00000231228.3:c.892G= MANE Select | ENSP00000231228.2:p.Val298= | |
| ENST00000231228.2:c.892G= | ENSP00000231228.2:p.Val298= | |
| NM_002187.2:c.892G= , LRG_71t1:c.892G= | NP_002178.2:p.Val298= | |
| NM_002187.3:c.892G= MANE Select | NP_002178.2:p.Val298= |