Linked Data
ClinVar Variation Id:
2184377
ClinVar RCV Id:
RCV002615778
dbSNP Id:
rs368180043
ExAC:
13:52520605 T / C
gnomAD v2:
13-52520605-T-C
gnomAD v4:
13-51946469-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51946469T>C , CM000675.2:g.51946469T>C | GRCh38 |
| NC_000013.10:g.52520605T>C , CM000675.1:g.52520605T>C | GRCh37 |
| NC_000013.9:g.51418606T>C | NCBI36 |
| NG_008806.1:g.70026A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*708A>G | ENSP00000489512.2:n.*708A>G | |
| ENST00000673864.2:c.*1619A>G | ENSP00000501045.2:n.*1619A>G | |
| ENST00000674147.2:c.2254A>G | ENSP00000500964.2:p.Lys752Glu | |
| ENST00000242839.10:c.2875A>G MANE Select | ENSP00000242839.5:p.Lys959Glu | |
| ENST00000344297.9:c.2254A>G | ENSP00000342559.5:p.Lys752Glu | |
| ENST00000400366.6:c.2542A>G | ENSP00000383217.3:p.Lys848Glu | |
| ENST00000448424.7:c.2623A>G | ENSP00000416738.3:p.Lys875Glu | |
| ENST00000673772.1:c.2641A>G | ENSP00000501168.1:p.Lys881Glu | |
| ENST00000673867.1:n.1022A>G | ||
| ENST00000674126.1:n.3238A>G | ||
| ENST00000674147.1:c.1810A>G | ENSP00000500964.1:p.Lys604Glu | |
| ENST00000242839.8:c.2875A>G | ENSP00000242839.4:p.Lys959Glu | |
| ENST00000344297.8:c.2254A>G | ENSP00000342559.5:p.Lys752Glu | |
| ENST00000400366.5:c.2542A>G | ENSP00000383217.3:p.Lys848Glu | |
| ENST00000400370.8:c.1585A>G | ENSP00000383221.3:p.Lys529Glu | |
| ENST00000418097.7:c.2866-2178A>G | ENSP00000393343.2:n.2866-2178A>G | |
| ENST00000448424.6:c.2641A>G | ENSP00000416738.2:p.Lys881Glu | |
| ENST00000466629.1:n.95A>G | ||
| ENST00000634296.1:c.836A>G | ||
| ENST00000634308.1:c.2661A>G | ENSP00000489234.1:p.Thr887= | |
| ENST00000634620.1:n.3619A>G | ||
| ENST00000634810.1:n.2220A>G | ||
| ENST00000634844.1:c.2731A>G | ENSP00000489398.1:p.Lys911Glu | |
| ENST00000635406.1:n.221A>G | ||
| NM_000053.3:c.2875A>G | NP_000044.2:p.Lys959Glu | |
| NM_001005918.2:c.2254A>G | NP_001005918.1:p.Lys752Glu | |
| NM_001243182.1:c.2542A>G | NP_001230111.1:p.Lys848Glu | |
| XM_005266423.2:c.2779A>G | XP_005266480.1:p.Lys927Glu | |
| XM_005266424.3:c.2779A>G | XP_005266481.1:p.Lys927Glu | |
| XM_005266427.2:c.2641A>G | XP_005266484.1:p.Lys881Glu | |
| XM_005266428.1:c.2623A>G | XP_005266485.1:p.Lys875Glu | |
| XM_005266430.3:c.2875A>G | XP_005266487.1:p.Lys959Glu | |
| XM_005266431.2:c.2839A>G | XP_005266488.1:p.Lys947Glu | |
| XM_005266432.2:c.2389A>G | XP_005266489.1:p.Lys797Glu | |
| XM_006719837.2:c.2779A>G | XP_006719900.1:p.Lys927Glu | |
| XM_006719838.1:c.691A>G | XP_006719901.1:p.Lys231Glu | |
| XM_006719839.1:c.691A>G | XP_006719902.1:p.Lys231Glu | |
| XM_011535117.1:c.2779A>G | XP_011533419.1:p.Lys927Glu | |
| XM_011535118.1:c.2740A>G | XP_011533420.1:p.Lys914Glu | |
| XM_011535119.1:c.2875A>G | XP_011533421.1:p.Lys959Glu | |
| XM_011535120.1:c.2461A>G | XP_011533422.1:p.Lys821Glu | |
| XM_011535121.1:c.2730+3538A>G | XP_011533423.1:n.2730+3538A>G | |
| XM_011535122.1:c.1543A>G | XP_011533424.1:p.Lys515Glu | |
| XR_941601.1:n.3094A>G | ||
| XR_941602.1:n.3094A>G | ||
| XR_941603.1:n.3094A>G | ||
| XR_941604.1:n.3094A>G | ||
| NM_001330578.1:c.2641A>G | NP_001317507.1:p.Lys881Glu | |
| NM_001330579.1:c.2623A>G | NP_001317508.1:p.Lys875Glu | |
| XM_005266424.4:c.2779A>G | XP_005266481.1:p.Lys927Glu | |
| XM_005266430.4:c.2875A>G | XP_005266487.1:p.Lys959Glu | |
| XM_005266431.4:c.2839A>G | XP_005266488.1:p.Lys947Glu | |
| XM_006719837.3:c.2779A>G | XP_006719900.1:p.Lys927Glu | |
| XM_011535117.3:c.2779A>G | XP_011533419.1:p.Lys927Glu | |
| XM_017020627.1:c.2779A>G | XP_016876116.1:p.Lys927Glu | |
| NM_000053.4:c.2875A>G MANE Select | NP_000044.2:p.Lys959Glu | |
| NM_001005918.3:c.2254A>G | NP_001005918.1:p.Lys752Glu | |
| NM_001330579.2:c.2623A>G | NP_001317508.1:p.Lys875Glu | |
| NM_001243182.2:c.2542A>G | NP_001230111.1:p.Lys848Glu | |
| NM_001330578.2:c.2641A>G | NP_001317507.1:p.Lys881Glu |