Linked Data
ClinVar Variation Id:
876472
dbSNP Id:
rs1387034807
gnomAD v4:
1-226895477-C-T
MyVariant Identifiers:
chr1:g.227083178C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.226895477C>T , CM000663.2:g.226895477C>T | GRCh38 |
| NC_000001.10:g.227083178C>T , CM000663.1:g.227083178C>T | GRCh37 |
| NC_000001.9:g.225149801C>T | NCBI36 |
| NG_007381.1:g.29906C>T | |
| NG_012825.2:g.2942C>T | |
| NG_007381.2:g.30294C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366779.6:c.1245C>T | ENSP00000355741.2:p.Ala415= | |
| ENST00000366782.6:c.1245C>T | ENSP00000355746.2:p.Ala415= | |
| ENST00000366783.8:c.1245C>T MANE Select | ENSP00000355747.3:p.Ala415= | |
| ENST00000471728.2:n.1883C>T | ||
| ENST00000524196.6:c.1245C>T | ENSP00000429036.2:p.Ala415= | |
| ENST00000626989.3:c.1245C>T | ENSP00000486498.2:p.Ala415= | |
| ENST00000676467.1:c.*1072C>T | ENSP00000504294.1:n.*1072C>T | |
| ENST00000676747.1:c.1188+1352C>T | ENSP00000503244.1:n.1188+1352C>T | |
| ENST00000676884.1:c.1245C>T | ENSP00000503200.1:p.Ala415= | |
| ENST00000676888.1:c.*586C>T | ENSP00000504483.1:n.*586C>T | |
| ENST00000676907.1:c.*824C>T | ENSP00000504410.1:n.*824C>T | |
| ENST00000676945.1:c.1191+1352C>T | ENSP00000504433.1:n.1191+1352C>T | |
| ENST00000677065.1:n.1806C>T | ||
| ENST00000677414.1:c.1245C>T | ENSP00000503116.1:p.Ala415= | |
| ENST00000677529.1:n.2975C>T | ||
| ENST00000677596.1:c.*1467C>T | ENSP00000503618.1:n.*1467C>T | |
| ENST00000677599.1:c.1191+1352C>T | ENSP00000503673.1:n.1191+1352C>T | |
| ENST00000677748.1:n.3500C>T | ||
| ENST00000677880.1:c.810C>T | ENSP00000503121.1:p.Ala270= | |
| ENST00000678021.1:c.*868C>T | ENSP00000504674.1:n.*868C>T | |
| ENST00000678233.1:c.1245C>T | ENSP00000504728.1:p.Ala415= | |
| ENST00000678320.1:c.1146C>T | ENSP00000503680.1:p.Ala382= | |
| ENST00000678655.1:c.1092+1352C>T | ENSP00000504230.1:n.1092+1352C>T | |
| ENST00000678706.1:c.*622C>T | ENSP00000503659.1:n.*622C>T | |
| ENST00000678776.1:c.*1382C>T | ENSP00000504624.1:n.*1382C>T | |
| ENST00000678784.1:c.1073-2243C>T | ENSP00000504652.1:n.1073-2243C>T | |
| ENST00000678820.1:c.1089+1352C>T | ENSP00000504138.1:n.1089+1352C>T | |
| ENST00000678835.1:c.*757-2243C>T | ENSP00000504343.1:n.*757-2243C>T | |
| ENST00000679088.1:c.1245C>T | ENSP00000504727.1:p.Ala415= | |
| ENST00000679098.1:c.1245C>T | ENSP00000504303.1:p.Ala415= | |
| ENST00000366782.5:c.1344C>T | ENSP00000355746.1:p.Ala448= | |
| ENST00000366783.7:c.1245C>T | ENSP00000355747.3:p.Ala415= | |
| ENST00000422240.6:c.1242C>T | ENSP00000403737.2:p.Ala414= | |
| ENST00000471728.1:n.503C>T | ||
| ENST00000472139.2:c.813C>T | ENSP00000427806.1:p.Ala271= | |
| ENST00000626989.2:c.1344C>T | ENSP00000486498.1:p.Ala448= | |
| NM_000447.2:c.1245C>T | NP_000438.2:p.Ala415= | |
| NM_012486.2:c.1242C>T | NP_036618.2:p.Ala414= | |
| XM_005273199.2:c.1245C>T | XP_005273256.1:p.Ala415= | |
| XM_011544236.1:c.813C>T | XP_011542538.1:p.Ala271= | |
| XR_949149.1:n.1979C>T | ||
| XM_005273199.4:c.1245C>T | XP_005273256.1:p.Ala415= | |
| XM_017001835.1:c.1245C>T | XP_016857324.1:p.Ala415= | |
| XM_017001836.1:c.1242C>T | XP_016857325.1:p.Ala414= | |
| XR_001737316.2:n.1478-2243C>T | ||
| XR_001737317.2:n.1478-2243C>T | ||
| XR_001737318.2:n.1960C>T | ||
| XR_001737319.1:n.2303C>T | ||
| XR_001737320.1:n.2300C>T | ||
| XR_001737321.1:n.1795C>T | ||
| XR_949149.2:n.1957C>T | ||
| XR_949150.3:n.2176C>T | ||
| NM_000447.3:c.1245C>T MANE Select | NP_000438.2:p.Ala415= | |
| NM_012486.3:c.1242C>T | NP_036618.2:p.Ala414= |