Linked Data
ClinVar Variation Id:
1562133
ClinVar RCV Id:
RCV002212378
dbSNP Id:
rs2135158047
gnomAD v3:
11-61366120-T-C
gnomAD v4:
11-61366120-T-C
MyVariant Identifiers:
chr11:g.61133592T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61366120T>C , CM000673.2:g.61366120T>C | GRCh38 |
| NC_000011.9:g.61133592T>C , CM000673.1:g.61133592T>C | GRCh37 |
| NC_000011.8:g.60890168T>C | NCBI36 |
| NG_032581.1:g.9120T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000451389.7:c.204T>C | ENSP00000508581.1:p.Ala68= | |
| ENST00000507563.7:c.146T>C | ENSP00000510363.1:p.Leu49Pro | |
| ENST00000540194.6:n.963T>C | ||
| ENST00000542946.2:c.204T>C | ENSP00000445792.1:p.Ala68= | |
| ENST00000543594.6:c.*415T>C | ENSP00000509354.1:n.*415T>C | |
| ENST00000685597.1:c.204T>C | ENSP00000509403.1:p.Ala68= | |
| ENST00000686820.1:c.146T>C | ENSP00000508587.1:p.Leu49Pro | |
| ENST00000688279.1:c.146T>C | ENSP00000510422.1:p.Leu49Pro | |
| ENST00000688430.1:n.130T>C | ||
| ENST00000689076.1:c.204T>C | ENSP00000508469.1:p.Ala68= | |
| ENST00000689882.1:c.146T>C | ENSP00000509351.1:p.Leu49Pro | |
| ENST00000691720.1:c.204T>C | ENSP00000509146.1:p.Ala68= | |
| ENST00000692219.1:c.204T>C | ENSP00000510149.1:p.Ala68= | |
| ENST00000692667.1:c.204T>C | ENSP00000510180.1:p.Ala68= | |
| ENST00000692785.1:c.204T>C | ENSP00000509310.1:p.Ala68= | |
| ENST00000693557.1:c.204T>C | ENSP00000508970.1:p.Ala68= | |
| ENST00000278826.11:c.204T>C MANE Select | ENSP00000278826.5:p.Ala68= | |
| ENST00000278826.10:c.204T>C | ENSP00000278826.5:p.Ala68= | |
| ENST00000381787.2:c.30T>C | ENSP00000371206.2:p.Ala10= | |
| ENST00000423772.6:n.1723T>C | ||
| ENST00000451389.6:n.345T>C | ||
| ENST00000507563.6:n.377T>C | ||
| ENST00000534963.5:n.303T>C | ||
| ENST00000540194.5:n.378T>C | ||
| ENST00000542946.1:c.204T>C | ENSP00000445792.1:p.Ala68= | |
| ENST00000545420.1:n.228T>C | ||
| NM_016464.4:c.204T>C | NP_057548.1:p.Ala68= | |
| NR_028473.1:n.646T>C | ||
| XM_006718585.2:c.204T>C | XP_006718648.1:p.Ala68= | |
| XM_006718586.1:c.204T>C | XP_006718649.1:p.Ala68= | |
| XM_006718588.2:c.30T>C | XP_006718651.1:p.Ala10= | |
| XM_011545098.1:c.204T>C | XP_011543400.1:p.Ala68= | |
| XM_011545099.1:c.204T>C | XP_011543401.1:p.Ala68= | |
| XM_011545100.1:c.204T>C | XP_011543402.1:p.Ala68= | |
| XR_949964.1:n.403T>C | ||
| XR_949965.1:n.403T>C | ||
| XR_949966.1:n.403T>C | ||
| NM_001330281.1:c.30T>C | NP_001317210.1:p.Ala10= | |
| XM_006718585.3:c.204T>C | XP_006718648.1:p.Ala68= | |
| XM_006718586.2:c.204T>C | XP_006718649.1:p.Ala68= | |
| XM_011545098.2:c.204T>C | XP_011543400.1:p.Ala68= | |
| XM_011545099.2:c.204T>C | XP_011543401.1:p.Ala68= | |
| XM_017017917.1:c.204T>C | XP_016873406.1:p.Ala68= | |
| XR_949964.3:n.403T>C | ||
| XR_949966.2:n.403T>C | ||
| NM_016464.5:c.204T>C MANE Select | NP_057548.1:p.Ala68= | |
| NM_001330281.2:c.30T>C | NP_001317210.1:p.Ala10= | |
| NR_028473.2:n.273T>C |