Linked Data
ClinVar Variation Id:
214286
dbSNP Id:
rs748597500
ExAC:
2:74177859 G / A
gnomAD v2:
2-74177859-G-A
gnomAD v3:
2-73950732-G-A
gnomAD v4:
2-73950732-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73950732G>A , CM000664.2:g.73950732G>A | GRCh38 |
| NC_000002.11:g.74177859G>A , CM000664.1:g.74177859G>A | GRCh37 |
| NC_000002.10:g.74031367G>A | NCBI36 |
| NG_008044.1:g.28907G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264093.9:c.591G>A MANE Select | ENSP00000264093.4:p.Gln197= | |
| ENST00000264093.8:c.591G>A | ENSP00000264093.4:p.Gln197= | |
| ENST00000348222.3:c.443+3826G>A | ENSP00000306964.3:n.443+3826G>A | |
| ENST00000418996.5:c.*60+3826G>A | ENSP00000408209.1:n.*60+3826G>A | |
| ENST00000462685.1:n.536G>A | ||
| ENST00000489796.5:n.592G>A | ||
| ENST00000629438.2:c.*208G>A | ENSP00000487122.1:n.*208G>A | |
| NM_080916.2:c.591G>A | NP_550438.1:p.Gln197= | |
| NM_080918.2:c.443+3826G>A | NP_550440.1:n.443+3826G>A | |
| XM_005264173.2:c.300G>A | XP_005264230.1:p.Gln100= | |
| XM_005264174.1:c.300G>A | XP_005264231.1:p.Gln100= | |
| XM_011532647.1:c.573G>A | XP_011530949.1:p.Gln191= | |
| XM_011532648.1:c.282G>A | XP_011530950.1:p.Gln94= | |
| XR_244926.2:n.672G>A | ||
| NM_001318859.1:c.425+3844G>A | NP_001305788.1:n.425+3844G>A | |
| NM_001318860.1:c.300G>A | NP_001305789.1:p.Gln100= | |
| NM_001318861.1:c.300G>A | NP_001305790.1:p.Gln100= | |
| NM_001318862.1:c.282G>A | NP_001305791.1:p.Gln94= | |
| NM_001318863.1:c.282G>A | NP_001305792.1:p.Gln94= | |
| NR_134893.1:n.415+3826G>A | ||
| NR_134894.1:n.563G>A | ||
| NR_134895.1:n.228-7414G>A | ||
| NR_134896.1:n.397+3844G>A | ||
| NR_134897.1:n.607G>A | ||
| NR_134898.1:n.415+3826G>A | ||
| XM_011532647.2:c.573G>A | XP_011530949.1:p.Gln191= | |
| XM_024452739.1:c.300G>A | XP_024308507.1:p.Gln100= | |
| XR_001738656.1:n.527+3826G>A | ||
| XR_244926.3:n.674G>A | ||
| NM_080916.3:c.591G>A MANE Select | NP_550438.1:p.Gln197= | |
| NM_001318859.2:c.425+3844G>A | NP_001305788.1:n.425+3844G>A | |
| NM_001318860.2:c.300G>A | NP_001305789.1:p.Gln100= | |
| NM_001318861.2:c.300G>A | NP_001305790.1:p.Gln100= | |
| NM_001318862.2:c.282G>A | NP_001305791.1:p.Gln94= | |
| NM_001318863.2:c.282G>A | NP_001305792.1:p.Gln94= | |
| NM_080918.3:c.443+3826G>A | NP_550440.1:n.443+3826G>A | |
| NR_134893.2:n.361+3826G>A | ||
| NR_134894.2:n.509G>A | ||
| NR_134895.2:n.174-7414G>A | ||
| NR_134896.2:n.343+3844G>A | ||
| NR_134897.2:n.553G>A | ||
| NR_134898.2:n.361+3826G>A |