Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16992504T= , CM000670.2:g.16992504T= | GRCh38 |
| NC_000008.10:g.16850013T= , CM000670.1:g.16850013T= | GRCh37 |
| NC_000008.9:g.16894384T= | NCBI36 |
| NG_015978.1:g.14662A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.*568A= MANE Select | ENSP00000180166.5:n.*568A= | |
| ENST00000180166.5:c.*568A= | ENSP00000180166.5:n.*568A= | |
| NM_019851.3:c.*568A= MANE Select | NP_062825.1:n.*568A= |