MyVariant.info:
GRCh38
chr15:g.28272372G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.28272372G>C , CM000677.2:g.28272372G>C | GRCh38 |
| NC_000015.8:g.26191113G>C | NCBI36 |
| NG_016355.1:g.54778C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261609.13:c.926C>G MANE Select | ENSP00000261609.8:p.Ala309Gly | |
| ENST00000261609.11:c.926C>G | ENSP00000261609.7:p.Ala309Gly | |
| ENST00000563670.1:n.290C>G | ||
| ENST00000564734.5:c.*796C>G | ENSP00000456237.1:n.*796C>G | |
| NM_004667.5:c.926C>G | NP_004658.3:p.Ala309Gly | |
| XM_005268276.3:c.812C>G | XP_005268333.1:p.Ala271Gly | |
| XM_005268277.3:c.812C>G | XP_005268334.1:p.Ala271Gly | |
| XM_006720726.2:c.926C>G | XP_006720789.1:p.Ala309Gly | |
| XM_006720727.2:c.668C>G | XP_006720790.1:p.Ala223Gly | |
| XM_011522131.1:c.443C>G | XP_011520433.1:p.Ala148Gly | |
| XM_011522132.1:c.-51C>G | XP_011520434.1:n.-51C>G | |
| XM_011522133.1:c.322+20516C>G | XP_011520435.1:n.322+20516C>G | |
| XM_011522135.1:c.926C>G | XP_011520437.1:p.Ala309Gly | |
| XM_011522136.1:c.926C>G | XP_011520438.1:p.Ala309Gly | |
| XM_011522137.1:c.926C>G | XP_011520439.1:p.Ala309Gly | |
| XR_931930.1:n.1055C>G | ||
| XR_931931.1:n.1055C>G | ||
| XM_005268276.5:c.812C>G | XP_005268333.1:p.Ala271Gly | |
| XM_006720726.3:c.926C>G | XP_006720789.1:p.Ala309Gly | |
| XM_006720727.3:c.668C>G | XP_006720790.1:p.Ala223Gly | |
| XM_017022695.1:c.812C>G | XP_016878184.1:p.Ala271Gly | |
| XM_017022696.1:c.812C>G | XP_016878185.1:p.Ala271Gly | |
| XR_001751410.1:n.1056C>G | ||
| XR_931930.2:n.1056C>G | ||
| NM_004667.6:c.926C>G MANE Select | NP_004658.3:p.Ala309Gly |