Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16992623A= , CM000670.2:g.16992623A= | GRCh38 |
| NC_000008.10:g.16850132A= , CM000670.1:g.16850132A= | GRCh37 |
| NC_000008.9:g.16894503A= | NCBI36 |
| NG_015978.1:g.14543T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.*449T= MANE Select | ENSP00000180166.5:n.*449T= | |
| ENST00000180166.5:c.*449T= | ENSP00000180166.5:n.*449T= | |
| NM_019851.3:c.*449T= MANE Select | NP_062825.1:n.*449T= |