Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20192664G= , CM000675.2:g.20192664G= | GRCh38 |
| NC_000013.10:g.20766803G= , CM000675.1:g.20766803G= | GRCh37 |
| NC_000013.9:g.19664803G= | NCBI36 |
| NG_008358.1:g.5312C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382848.5:c.-23+119C= MANE Select | ENSP00000372299.4:n.-23+119C= | |
| ENST00000382848.4:c.-23+119C= | ENSP00000372299.4:n.-23+119C= | |
| NM_004004.5:c.-23+119C= | NP_003995.2:n.-23+119C= | |
| NM_004004.6:c.-23+119C= MANE Select | NP_003995.2:n.-23+119C= |