Linked Data
ClinVar Variation Id:
1369489
dbSNP Id:
rs200100285
ExAC:
1:11856370 T / C
gnomAD v2:
1-11856370-T-C
gnomAD v3:
1-11796313-T-C
gnomAD v4:
1-11796313-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11796313T>C , CM000663.2:g.11796313T>C | GRCh38 |
| NC_000001.10:g.11856370T>C , CM000663.1:g.11856370T>C | GRCh37 |
| NC_000001.9:g.11778957T>C | NCBI36 |
| NG_013351.1:g.14791A>G , LRG_726:g.14791A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376486.3:c.673A>G | ENSP00000365669.3:p.Ile225Val | |
| ENST00000376585.6:c.796A>G | ENSP00000365770.1:p.Ile266Val | |
| ENST00000376590.9:c.673A>G MANE Select | ENSP00000365775.3:p.Ile225Val | |
| ENST00000376592.6:c.673A>G | ENSP00000365777.1:p.Ile225Val | |
| ENST00000423400.7:c.793A>G | ENSP00000398908.3:p.Ile265Val | |
| ENST00000641407.1:c.673A>G | ENSP00000493098.1:p.Ile225Val | |
| ENST00000641446.1:c.673A>G | ENSP00000493262.1:p.Ile225Val | |
| ENST00000641721.1:n.644-965A>G | ||
| ENST00000641747.1:c.*185A>G | ENSP00000493116.1:n.*185A>G | |
| ENST00000641759.1:n.808A>G | ||
| ENST00000641805.1:n.956A>G | ||
| ENST00000641820.1:c.-63A>G | ENSP00000492937.1:n.-63A>G | |
| ENST00000376583.7:c.796A>G | ENSP00000365767.3:p.Ile266Val | |
| ENST00000376585.5:c.796A>G | ENSP00000365770.1:p.Ile266Val | |
| ENST00000376590.7:c.673A>G | ENSP00000365775.3:p.Ile225Val | |
| ENST00000376592.5:c.673A>G | ENSP00000365777.1:p.Ile225Val | |
| NM_005957.4:c.673A>G , LRG_726t1:c.673A>G | NP_005948.3:p.Ile225Val | |
| XM_005263458.2:c.796A>G | XP_005263515.1:p.Ile266Val | |
| XM_005263460.3:c.673A>G | XP_005263517.1:p.Ile225Val | |
| XM_005263461.3:c.673A>G | XP_005263518.1:p.Ile225Val | |
| XM_005263462.3:c.673A>G | XP_005263519.1:p.Ile225Val | |
| XM_005263463.2:c.427A>G | XP_005263520.1:p.Ile143Val | |
| XM_011541495.1:c.793A>G | XP_011539797.1:p.Ile265Val | |
| XM_011541496.1:c.796A>G | XP_011539798.1:p.Ile266Val | |
| NM_001330358.1:c.796A>G | NP_001317287.1:p.Ile266Val | |
| XM_005263460.5:c.673A>G | XP_005263517.1:p.Ile225Val | |
| XM_005263462.4:c.673A>G | XP_005263519.1:p.Ile225Val | |
| XM_005263463.4:c.427A>G | XP_005263520.1:p.Ile143Val | |
| XM_011541495.3:c.793A>G | XP_011539797.1:p.Ile265Val | |
| XM_011541496.3:c.796A>G | XP_011539798.1:p.Ile266Val | |
| XM_017001328.2:c.796A>G | XP_016856817.1:p.Ile266Val | |
| XM_024447198.1:c.427A>G | XP_024302966.1:p.Ile143Val | |
| XR_002956640.1:n.1540A>G | ||
| NM_005957.5:c.673A>G MANE Select | NP_005948.3:p.Ile225Val | |
| NM_001330358.2:c.796A>G | NP_001317287.1:p.Ile266Val |