Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.55655632A= , CM000678.2:g.55655632A= | GRCh38 |
| NC_000016.9:g.55689544A= , CM000678.1:g.55689544A= | GRCh37 |
| NC_000016.8:g.54247045A= | NCBI36 |
| NG_016969.1:g.5003A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001172501.1:c.-589A= | NP_001165972.1:n.-589A= |
| ENST00000568943.5:c.-589A= | ENSP00000457473.1:n.-589A= |
| XM_011523295.1:c.-589A= | XP_011521597.1:n.-589A= |
| XM_011523296.1:c.-589A= | XP_011521598.1:n.-589A= |
| XM_011523297.1:c.-589A= | XP_011521599.1:n.-589A= |
| XM_011523298.1:c.-589A= | XP_011521600.1:n.-589A= |
| XR_933403.1:n.29A= | |
| XR_933603.1:n.21T= |