Linked Data
ClinVar Variation Id:
98207
dbSNP Id:
rs1052553
ExAC:
17:44073889 A / G
gnomAD v2:
17-44073889-A-G
gnomAD v3:
17-45996523-A-G
gnomAD v4:
17-45996523-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.45996523A>G , CM000679.2:g.45996523A>G | GRCh38 |
| NC_000017.10:g.44073889A>G , CM000679.1:g.44073889A>G | GRCh37 |
| NC_000017.9:g.41429726A>G | NCBI36 |
| NG_007398.1:g.107103A>G | |
| NG_007398.2:g.107061A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000420682.7:c.594A>G | ENSP00000413056.2:p.Ala198= | |
| ENST00000703922.1:c.594A>G | ENSP00000515557.1:p.Ala198= | |
| ENST00000703923.1:c.507A>G | ENSP00000515558.1:p.Ala169= | |
| ENST00000703924.1:c.594A>G | ENSP00000515559.1:p.Ala198= | |
| ENST00000703978.1:c.681A>G | ENSP00000515600.1:p.Ala227= | |
| ENST00000703979.1:n.545A>G | ||
| ENST00000262410.10:c.1857A>G MANE Select | ENSP00000262410.6:p.Ala619= | |
| ENST00000344290.10:c.1659A>G | ENSP00000340820.6:p.Ala553= | |
| ENST00000351559.10:c.681A>G | ENSP00000303214.7:p.Ala227= | |
| ENST00000535772.6:c.594A>G | ENSP00000443028.2:p.Ala198= | |
| ENST00000680542.1:c.594A>G | ENSP00000505258.1:p.Ala198= | |
| ENST00000680674.1:c.507A>G | ENSP00000505478.1:p.Ala169= | |
| ENST00000262410.9:c.1632A>G | ENSP00000262410.5:p.Ala544= | |
| ENST00000334239.12:c.507A>G | ENSP00000334886.8:p.Ala169= | |
| ENST00000340799.9:c.594A>G | ENSP00000340438.5:p.Ala198= | |
| ENST00000344290.9:c.1686A>G | ENSP00000340820.5:p.Ala562= | |
| ENST00000351559.9:c.681A>G | ENSP00000303214.7:p.Ala227= | |
| ENST00000415613.6:c.1686A>G | ENSP00000410838.2:p.Ala562= | |
| ENST00000420682.6:c.594A>G | ENSP00000413056.2:p.Ala198= | |
| ENST00000431008.7:c.681A>G | ENSP00000389250.3:p.Ala227= | |
| ENST00000446361.7:c.507A>G | ENSP00000408975.3:p.Ala169= | |
| ENST00000535772.5:c.681A>G | ENSP00000443028.1:p.Ala227= | |
| ENST00000570299.5:n.635A>G | ||
| ENST00000571987.5:c.1632A>G | ENSP00000458742.1:p.Ala544= | |
| ENST00000574436.5:c.681A>G | ENSP00000460965.1:p.Ala227= | |
| ENST00000576518.1:n.5966A>G | ||
| NM_001123066.3:c.1686A>G | NP_001116538.2:p.Ala562= | |
| NM_001123067.3:c.594A>G | NP_001116539.1:p.Ala198= | |
| NM_001203251.1:c.594A>G | NP_001190180.1:p.Ala198= | |
| NM_001203252.1:c.681A>G | NP_001190181.1:p.Ala227= | |
| NM_005910.5:c.681A>G | NP_005901.2:p.Ala227= | |
| NM_016834.4:c.507A>G | NP_058518.1:p.Ala169= | |
| NM_016835.4:c.1632A>G | NP_058519.3:p.Ala544= | |
| NM_016841.4:c.507A>G | NP_058525.1:p.Ala169= | |
| XM_005257362.3:c.1944A>G | XP_005257419.1:p.Ala648= | |
| XM_005257364.3:c.1857A>G | XP_005257421.1:p.Ala619= | |
| XM_005257365.3:c.1944A>G | XP_005257422.1:p.Ala648= | |
| XM_005257366.2:c.1770A>G | XP_005257423.1:p.Ala590= | |
| XM_005257367.3:c.1746A>G | XP_005257424.1:p.Ala582= | |
| XM_005257368.3:c.1746A>G | XP_005257425.1:p.Ala582= | |
| XM_005257369.3:c.879A>G | XP_005257426.1:p.Ala293= | |
| XM_005257370.3:c.792A>G | XP_005257427.1:p.Ala264= | |
| XM_005257371.3:c.705A>G | XP_005257428.1:p.Ala235= | |
| XM_005257362.4:c.1944A>G | XP_005257419.1:p.Ala648= | |
| XM_005257364.4:c.1857A>G | XP_005257421.1:p.Ala619= | |
| XM_005257365.4:c.1944A>G | XP_005257422.1:p.Ala648= | |
| XM_005257366.3:c.1770A>G | XP_005257423.1:p.Ala590= | |
| XM_005257367.4:c.1746A>G | XP_005257424.1:p.Ala582= | |
| XM_005257368.4:c.1746A>G | XP_005257425.1:p.Ala582= | |
| XM_005257369.4:c.879A>G | XP_005257426.1:p.Ala293= | |
| XM_005257370.4:c.792A>G | XP_005257427.1:p.Ala264= | |
| XM_005257371.4:c.705A>G | XP_005257428.1:p.Ala235= | |
| NM_001203251.2:c.594A>G | NP_001190180.1:p.Ala198= | |
| NM_001377265.1:c.1857A>G MANE Select | NP_001364194.1:p.Ala619= | |
| NM_001377266.1:c.1659A>G | NP_001364195.1:p.Ala553= | |
| NM_001377267.1:c.594A>G | NP_001364196.1:p.Ala198= | |
| NM_001377268.1:c.507A>G | NP_001364197.1:p.Ala169= | |
| NM_016834.5:c.507A>G | NP_058518.1:p.Ala169= | |
| NM_016841.5:c.507A>G | NP_058525.1:p.Ala169= | |
| NR_165166.1:n.605A>G | ||
| NM_001123066.4:c.1686A>G | NP_001116538.2:p.Ala562= | |
| NM_001123067.4:c.594A>G | NP_001116539.1:p.Ala198= | |
| NM_001203252.2:c.681A>G | NP_001190181.1:p.Ala227= | |
| NM_005910.6:c.681A>G | NP_005901.2:p.Ala227= | |
| NM_016835.5:c.1632A>G | NP_058519.3:p.Ala544= |