Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108147606T= , CM000673.2:g.108147606T= | GRCh38 |
| NC_000011.9:g.108018333T= , CM000673.1:g.108018333T= | GRCh37 |
| NC_000011.8:g.107523543T= | NCBI36 |
| NG_009888.1:g.31076T= | |
| NG_009888.2:g.35902T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265838.8:c.*216T= | ENSP00000265838.4:n.*216T= | |
| NM_000019.3:c.*216T= | NP_000010.1:n.*216T= | |
| XM_006718834.2:c.*216T= | XP_006718897.1:n.*216T= | |
| XM_006718835.2:c.*216T= | XP_006718898.1:n.*216T= | |
| XM_017017682.2:c.*216T= | XP_016873171.1:n.*216T= | |
| XM_017017683.2:c.*216T= | XP_016873172.1:n.*216T= |