Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117807303C= , CM000670.2:g.117807303C= | GRCh38 |
| NC_000008.10:g.118819542C= , CM000670.1:g.118819542C= | GRCh37 |
| NC_000008.9:g.118888723C= | NCBI36 |
| NG_007455.2:g.309517G= , LRG_493:g.309517G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.1264G= | ||
| ENST00000378204.7:c.1797G= MANE Select | ENSP00000367446.3:p.Trp599= | |
| ENST00000378204.6:c.1797G= | ENSP00000367446.2:p.Trp599= | |
| ENST00000437196.1:c.*688G= | ENSP00000407299.1:n.*688G= | |
| NM_000127.2:c.1797G= , LRG_493t1:c.1797G= | NP_000118.2:p.Trp599= | |
| NM_000127.3:c.1797G= MANE Select | NP_000118.2:p.Trp599= |