Linked Data
ClinVar Variation Id:
476776
dbSNP Id:
rs201474903
ExAC:
1:10342521 C / T
gnomAD v2:
1-10342521-C-T
gnomAD v3:
1-10282463-C-T
gnomAD v4:
1-10282463-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.10282463C>T , CM000663.2:g.10282463C>T | GRCh38 |
| NC_000001.10:g.10342521C>T , CM000663.1:g.10342521C>T | GRCh37 |
| NC_000001.9:g.10265108C>T | NCBI36 |
| NG_008069.1:g.76758C>T , LRG_252:g.76758C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696500.1:c.*398C>T | ENSP00000512666.1:n.*398C>T | |
| ENST00000696502.1:c.1226C>T | ENSP00000512668.1:p.Thr409Met | |
| ENST00000696503.1:c.1226C>T | ENSP00000512669.1:p.Thr409Met | |
| ENST00000696504.1:c.1226C>T | ENSP00000512670.1:p.Thr409Met | |
| ENST00000696507.1:c.64C>T | ||
| ENST00000377093.9:c.1226C>T | ENSP00000366297.4:p.Thr409Met | |
| ENST00000676179.1:c.1364C>T MANE Select | ENSP00000502065.1:p.Thr455Met | |
| ENST00000263934.10:c.1226C>T | ENSP00000263934.6:p.Thr409Met | |
| ENST00000377081.5:c.1364C>T | ENSP00000366284.1:p.Thr455Met | |
| ENST00000377083.5:c.1226C>T | ENSP00000366287.1:p.Thr409Met | |
| ENST00000377086.5:c.1364C>T | ENSP00000366290.1:p.Thr455Met | |
| ENST00000377093.8:c.1226C>T | ENSP00000366297.4:p.Thr409Met | |
| ENST00000497835.1:n.14C>T | ||
| ENST00000620295.2:c.1322C>T | ENSP00000478500.1:p.Thr441Met | |
| ENST00000622724.3:c.1286C>T | ENSP00000480063.1:p.Thr429Met | |
| NM_015074.3:c.1226C>T , LRG_252t1:c.1226C>T | NP_055889.2:p.Thr409Met | |
| NM_183416.3:c.1226C>T | NP_904325.2:p.Thr409Met | |
| NM_001365951.1:c.1364C>T | NP_001352880.1:p.Thr455Met | |
| NM_001365952.1:c.1364C>T | NP_001352881.1:p.Thr455Met | |
| NM_001365953.1:c.1226C>T | NP_001352882.1:p.Thr409Met | |
| NM_001365951.3:c.1364C>T MANE Select | NP_001352880.1:p.Thr455Met | |
| NM_183416.4:c.1226C>T | NP_904325.2:p.Thr409Met |