Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16992728A= , CM000670.2:g.16992728A= | GRCh38 |
| NC_000008.10:g.16850237A= , CM000670.1:g.16850237A= | GRCh37 |
| NC_000008.9:g.16894608A= | NCBI36 |
| NG_015978.1:g.14438T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.*344T= MANE Select | ENSP00000180166.5:n.*344T= | |
| ENST00000180166.5:c.*344T= | ENSP00000180166.5:n.*344T= | |
| NM_019851.3:c.*344T= MANE Select | NP_062825.1:n.*344T= |