Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108084705C= , CM000685.2:g.108084705C= | GRCh38 |
| NC_000023.10:g.107327935C= , CM000685.1:g.107327935C= | GRCh37 |
| NC_000023.9:g.107214591C= | NCBI36 |
| NG_012521.1:g.11914G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217958.8:c.*269G= MANE Select | ENSP00000217958.3:n.*269G= | |
| ENST00000217958.7:c.*269G= | ENSP00000217958.3:n.*269G= | |
| ENST00000372296.5:c.*415G= | ENSP00000361370.1:n.*415G= | |
| NM_002814.3:c.*269G= | NP_002805.1:n.*269G= | |
| NM_170750.2:c.*415G= | NP_736606.1:n.*415G= | |
| NM_002814.4:c.*269G= MANE Select | NP_002805.1:n.*269G= | |
| NM_170750.3:c.*415G= | NP_736606.1:n.*415G= |