Linked Data
ClinVar Variation Id:
1346683
ClinVar RCV Id:
RCV002030138
dbSNP Id:
rs151048692
ExAC:
1:227083263 C / T
gnomAD v2:
1-227083263-C-T
gnomAD v3:
1-226895562-C-T
gnomAD v4:
1-226895562-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.226895562C>T , CM000663.2:g.226895562C>T | GRCh38 |
| NC_000001.10:g.227083263C>T , CM000663.1:g.227083263C>T | GRCh37 |
| NC_000001.9:g.225149886C>T | NCBI36 |
| NG_007381.1:g.29991C>T | |
| NG_012825.2:g.3027C>T | |
| NG_007381.2:g.30379C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366779.6:c.1330C>T | ENSP00000355741.2:p.His444Tyr | |
| ENST00000366782.6:c.1330C>T | ENSP00000355746.2:p.His444Tyr | |
| ENST00000366783.8:c.1330C>T MANE Select | ENSP00000355747.3:p.His444Tyr | |
| ENST00000471728.2:n.1968C>T | ||
| ENST00000524196.6:c.1330C>T | ENSP00000429036.2:p.His444Tyr | |
| ENST00000626989.3:c.1330C>T | ENSP00000486498.2:p.His444Tyr | |
| ENST00000676467.1:c.*1157C>T | ENSP00000504294.1:n.*1157C>T | |
| ENST00000676747.1:c.1188+1437C>T | ENSP00000503244.1:n.1188+1437C>T | |
| ENST00000676884.1:c.1330C>T | ENSP00000503200.1:p.His444Tyr | |
| ENST00000676888.1:c.*671C>T | ENSP00000504483.1:n.*671C>T | |
| ENST00000676907.1:c.*909C>T | ENSP00000504410.1:n.*909C>T | |
| ENST00000676945.1:c.1191+1437C>T | ENSP00000504433.1:n.1191+1437C>T | |
| ENST00000677065.1:n.1891C>T | ||
| ENST00000677414.1:c.1330C>T | ENSP00000503116.1:p.His444Tyr | |
| ENST00000677529.1:n.3060C>T | ||
| ENST00000677596.1:c.*1552C>T | ENSP00000503618.1:n.*1552C>T | |
| ENST00000677599.1:c.1191+1437C>T | ENSP00000503673.1:n.1191+1437C>T | |
| ENST00000677748.1:n.3585C>T | ||
| ENST00000677880.1:c.895C>T | ENSP00000503121.1:p.His299Tyr | |
| ENST00000678021.1:c.*953C>T | ENSP00000504674.1:n.*953C>T | |
| ENST00000678233.1:c.1330C>T | ENSP00000504728.1:p.His444Tyr | |
| ENST00000678320.1:c.1231C>T | ENSP00000503680.1:p.His411Tyr | |
| ENST00000678655.1:c.1092+1437C>T | ENSP00000504230.1:n.1092+1437C>T | |
| ENST00000678706.1:c.*707C>T | ENSP00000503659.1:n.*707C>T | |
| ENST00000678776.1:c.*1467C>T | ENSP00000504624.1:n.*1467C>T | |
| ENST00000678784.1:c.1073-2158C>T | ENSP00000504652.1:n.1073-2158C>T | |
| ENST00000678820.1:c.1089+1437C>T | ENSP00000504138.1:n.1089+1437C>T | |
| ENST00000678835.1:c.*757-2158C>T | ENSP00000504343.1:n.*757-2158C>T | |
| ENST00000679088.1:c.1330C>T | ENSP00000504727.1:p.His444Tyr | |
| ENST00000679098.1:c.1330C>T | ENSP00000504303.1:p.His444Tyr | |
| ENST00000366782.5:c.1429C>T | ENSP00000355746.1:p.His477Tyr | |
| ENST00000366783.7:c.1330C>T | ENSP00000355747.3:p.His444Tyr | |
| ENST00000422240.6:c.1327C>T | ENSP00000403737.2:p.His443Tyr | |
| ENST00000472139.2:c.898C>T | ENSP00000427806.1:p.His300Tyr | |
| ENST00000626989.2:c.1429C>T | ENSP00000486498.1:p.His477Tyr | |
| NM_000447.2:c.1330C>T | NP_000438.2:p.His444Tyr | |
| NM_012486.2:c.1327C>T | NP_036618.2:p.His443Tyr | |
| XM_005273199.2:c.1330C>T | XP_005273256.1:p.His444Tyr | |
| XM_011544236.1:c.898C>T | XP_011542538.1:p.His300Tyr | |
| XM_005273199.4:c.1330C>T | XP_005273256.1:p.His444Tyr | |
| XM_017001835.1:c.1330C>T | XP_016857324.1:p.His444Tyr | |
| XM_017001836.1:c.1327C>T | XP_016857325.1:p.His443Tyr | |
| XR_001737316.2:n.1478-2158C>T | ||
| XR_001737317.2:n.1478-2158C>T | ||
| XR_001737318.2:n.2045C>T | ||
| XR_001737319.1:n.2388C>T | ||
| XR_001737320.1:n.2385C>T | ||
| XR_001737321.1:n.1880C>T | ||
| XR_949149.2:n.2042C>T | ||
| XR_949150.3:n.2261C>T | ||
| NM_000447.3:c.1330C>T MANE Select | NP_000438.2:p.His444Tyr | |
| NM_012486.3:c.1327C>T | NP_036618.2:p.His443Tyr |