Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118111540G= , CM000670.2:g.118111540G= | GRCh38 |
| NC_000008.10:g.119123779G= , CM000670.1:g.119123779G= | GRCh37 |
| NC_000008.9:g.119192960G= | NCBI36 |
| NG_007455.2:g.5280C= , LRG_493:g.5280C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378204.7:c.-494C= MANE Select | ENSP00000367446.3:n.-494C= | |
| ENST00000378204.6:c.-494C= | ENSP00000367446.2:n.-494C= | |
| NM_000127.2:c.-494C= , LRG_493t1:c.-494C= | NP_000118.2:n.-494C= | |
| NM_000127.3:c.-494C= MANE Select | NP_000118.2:n.-494C= |