Linked Data
ClinVar Variation Id:
2189756
dbSNP Id:
rs149514973
ExAC:
1:11861298 C / T
gnomAD v2:
1-11861298-C-T
gnomAD v3:
1-11801241-C-T
gnomAD v4:
1-11801241-C-T
COSMIC:
COSM894582
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11801241C>T , CM000663.2:g.11801241C>T | GRCh38 |
| NC_000001.10:g.11861298C>T , CM000663.1:g.11861298C>T | GRCh37 |
| NC_000001.9:g.11783885C>T | NCBI36 |
| NG_008766.1:g.92C>T | |
| NG_013351.1:g.9863G>A , LRG_726:g.9863G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376486.3:c.395G>A | ENSP00000365669.3:p.Arg132His | |
| ENST00000376585.6:c.518G>A | ENSP00000365770.1:p.Arg173His | |
| ENST00000376590.9:c.395G>A MANE Select | ENSP00000365775.3:p.Arg132His | |
| ENST00000376592.6:c.395G>A | ENSP00000365777.1:p.Arg132His | |
| ENST00000423400.7:c.515G>A | ENSP00000398908.3:p.Arg172His | |
| ENST00000641407.1:c.395G>A | ENSP00000493098.1:p.Arg132His | |
| ENST00000641437.1:n.527G>A | ||
| ENST00000641446.1:c.395G>A | ENSP00000493262.1:p.Arg132His | |
| ENST00000641721.1:n.452G>A | ||
| ENST00000641747.1:c.237-919G>A | ENSP00000493116.1:n.237-919G>A | |
| ENST00000641759.1:n.530G>A | ||
| ENST00000641805.1:n.678G>A | ||
| ENST00000641909.1:n.805G>A | ||
| ENST00000376583.7:c.518G>A | ENSP00000365767.3:p.Arg173His | |
| ENST00000376585.5:c.518G>A | ENSP00000365770.1:p.Arg173His | |
| ENST00000376590.7:c.395G>A | ENSP00000365775.3:p.Arg132His | |
| ENST00000376592.5:c.395G>A | ENSP00000365777.1:p.Arg132His | |
| ENST00000418034.1:c.395G>A | ENSP00000405082.1:p.Arg132His | |
| NM_005957.4:c.395G>A , LRG_726t1:c.395G>A | NP_005948.3:p.Arg132His | |
| XM_005263458.2:c.518G>A | XP_005263515.1:p.Arg173His | |
| XM_005263460.3:c.395G>A | XP_005263517.1:p.Arg132His | |
| XM_005263461.3:c.395G>A | XP_005263518.1:p.Arg132His | |
| XM_005263462.3:c.395G>A | XP_005263519.1:p.Arg132His | |
| XM_005263463.2:c.149G>A | XP_005263520.1:p.Arg50His | |
| XM_011541495.1:c.515G>A | XP_011539797.1:p.Arg172His | |
| XM_011541496.1:c.518G>A | XP_011539798.1:p.Arg173His | |
| NM_001330358.1:c.518G>A | NP_001317287.1:p.Arg173His | |
| XM_005263460.5:c.395G>A | XP_005263517.1:p.Arg132His | |
| XM_005263462.4:c.395G>A | XP_005263519.1:p.Arg132His | |
| XM_005263463.4:c.149G>A | XP_005263520.1:p.Arg50His | |
| XM_011541495.3:c.515G>A | XP_011539797.1:p.Arg172His | |
| XM_011541496.3:c.518G>A | XP_011539798.1:p.Arg173His | |
| XM_017001328.2:c.518G>A | XP_016856817.1:p.Arg173His | |
| XM_024447198.1:c.149G>A | XP_024302966.1:p.Arg50His | |
| XR_002956640.1:n.1262G>A | ||
| NM_005957.5:c.395G>A MANE Select | NP_005948.3:p.Arg132His | |
| NM_001330358.2:c.518G>A | NP_001317287.1:p.Arg173His |