Linked Data
dbSNP Id:
rs953897298
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57739351C>G , CM000674.2:g.57739351C>G | GRCh38 |
| NC_000012.11:g.58133134C>G , CM000674.1:g.58133134C>G | GRCh37 |
| NC_000012.10:g.56419401C>G | NCBI36 |
| NG_029755.1:g.7811G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257897.7:c.160+2561G>C (AGAP2) | ENSP00000257897.3:n.160+2561G>C | |
| ENST00000553221.5:n.189+1150C>G (TSPAN31) | ||
| NM_014770.3:c.160+2561G>C (AGAP2) | NP_055585.1:n.160+2561G>C | |
| XM_005268626.1:c.160+2561G>C (AGAP2) | XP_005268683.1:n.160+2561G>C | |
| XM_005268626.2:c.160+2561G>C (AGAP2) | XP_005268683.1:n.160+2561G>C | |
| NM_014770.4:c.160+2561G>C (AGAP2) | NP_055585.1:n.160+2561G>C |