Linked Data
gnomAD v4:
12-57739601-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57739601C>A , CM000674.2:g.57739601C>A | GRCh38 |
| NC_000012.11:g.58133384C>A , CM000674.1:g.58133384C>A | GRCh37 |
| NC_000012.10:g.56419651C>A | NCBI36 |
| NG_029755.1:g.7561G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257897.7:c.160+2311G>T (AGAP2) | ENSP00000257897.3:n.160+2311G>T | |
| ENST00000553221.5:n.189+1400C>A (TSPAN31) | ||
| NM_014770.3:c.160+2311G>T (AGAP2) | NP_055585.1:n.160+2311G>T | |
| XM_005268626.1:c.160+2311G>T (AGAP2) | XP_005268683.1:n.160+2311G>T | |
| XM_005268626.2:c.160+2311G>T (AGAP2) | XP_005268683.1:n.160+2311G>T | |
| NM_014770.4:c.160+2311G>T (AGAP2) | NP_055585.1:n.160+2311G>T |