Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48256972G= , CM000681.2:g.48256972G= | GRCh38 |
| NC_000019.9:g.48760229G= , CM000681.1:g.48760229G= | GRCh37 |
| NC_000019.8:g.53452041G= | NCBI36 |
| NG_029574.1:g.3975C= | |
| NG_029574.2:g.4298C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_040599.1:n.742G= (CARD8-AS1) | |
| ENST00000597695.1:c.-162+18987G= (ZNF114) | ENSP00000472747.1:n.-162+18987G= |