Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924727G= , CM000675.2:g.27924727G= | GRCh38 |
| NC_000013.10:g.28498864G= , CM000675.1:g.28498864G= | GRCh37 |
| NC_000013.9:g.27396864G= | NCBI36 |
| NG_008183.1:g.9697G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.*26G= MANE Select | ENSP00000370421.4:n.*26G= | |
| ENST00000381033.4:c.*26G= | ENSP00000370421.4:n.*26G= | |
| NM_000209.3:c.*26G= | NP_000200.1:n.*26G= | |
| NM_000209.4:c.*26G= MANE Select | NP_000200.1:n.*26G= |