Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118111538C= , CM000670.2:g.118111538C= | GRCh38 |
| NC_000008.10:g.119123777C= , CM000670.1:g.119123777C= | GRCh37 |
| NC_000008.9:g.119192958C= | NCBI36 |
| NG_007455.2:g.5282G= , LRG_493:g.5282G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378204.7:c.-492G= MANE Select | ENSP00000367446.3:n.-492G= | |
| ENST00000378204.6:c.-492G= | ENSP00000367446.2:n.-492G= | |
| NM_000127.2:c.-492G= , LRG_493t1:c.-492G= | NP_000118.2:n.-492G= | |
| NM_000127.3:c.-492G= MANE Select | NP_000118.2:n.-492G= |