Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57739585T= , CM000674.2:g.57739585T= | GRCh38 |
| NC_000012.11:g.58133368T= , CM000674.1:g.58133368T= | GRCh37 |
| NC_000012.10:g.56419635T= | NCBI36 |
| NG_029755.1:g.7577A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257897.7:c.160+2327A= (AGAP2) | ENSP00000257897.3:n.160+2327A= | |
| ENST00000553221.5:n.189+1384T= (TSPAN31) | ||
| NM_014770.3:c.160+2327A= (AGAP2) | NP_055585.1:n.160+2327A= | |
| XM_005268626.1:c.160+2327A= (AGAP2) | XP_005268683.1:n.160+2327A= | |
| XM_005268626.2:c.160+2327A= (AGAP2) | XP_005268683.1:n.160+2327A= | |
| NM_014770.4:c.160+2327A= (AGAP2) | NP_055585.1:n.160+2327A= |