Identifiers and link-outs to other resources
ClinVar Variation Id:
240769
ClinVar RCV Id:
RCV000228518
dbSNP Id:
rs878854929
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43094432T>C , CM000679.2:g.43094432T>C | GRCh38 |
| NC_000017.10:g.41246449T>C , CM000679.1:g.41246449T>C | GRCh37 |
| NC_000017.9:g.38499975T>C | NCBI36 |
| NG_005905.2:g.123552A>G , LRG_292:g.123552A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_007294.3:c.1099A>G , LRG_292t1:c.1099A>G | NP_009225.1:p.Thr367Ala | |
| NM_007297.3:c.958A>G VV | NP_009228.2:p.Thr320Ala | |
| NM_007298.3:c.787+312A>G VV | NP_009229.2:p.= | |
| NM_007299.3:c.787+312A>G VV | NP_009230.2:p.= | |
| NM_007300.3:c.1099A>G VV | NP_009231.2:p.Thr367Ala | |
| NR_027676.1:n.1235A>G | ||
| NM_007294.4:c.1099A>G VV MANE Preferred | NP_009225.1:p.Thr367Ala | |
| NM_007297.4:c.958A>G VV | NP_009228.2:p.Thr320Ala | |
| NM_007299.4:c.787+312A>G VV | NP_009230.2:p.= | |
| NM_007300.4:c.1099A>G VV | NP_009231.2:p.Thr367Ala | |
| NR_027676.2:n.1276A>G | ||
| ENST00000352993.7:c.670+1414A>G | ENSP00000312236.5:p.= | |
| ENST00000354071.7:c.1099A>G | ENSP00000326002.7:p.Thr367Ala | |
| ENST00000357654.7:c.1099A>G | ENSP00000350283.3:p.Thr367Ala | |
| ENST00000412061.3:n.450A>G | ||
| ENST00000461221.5:c.*882A>G | ENSP00000418548.1:p.= | |
| ENST00000468300.5:c.787+312A>G | ENSP00000417148.1:p.= | |
| ENST00000470026.5:c.1099A>G | ENSP00000419274.1:p.Thr367Ala | |
| ENST00000471181.6:c.1099A>G | ENSP00000418960.2:p.Thr367Ala | |
| ENST00000473961.5:n.696A>G | ||
| ENST00000477152.5:c.1021A>G | ENSP00000419988.1:p.Thr341Ala | |
| ENST00000478531.5:c.784+312A>G | ENSP00000420412.1:p.= | |
| ENST00000484087.5:n.409+312A>G | ENSP00000419481.1:p.= | |
| ENST00000487825.5:n.412+312A>G | ENSP00000418212.1:p.= | |
| ENST00000491747.6:c.787+312A>G | ENSP00000420705.2:p.= | |
| ENST00000492859.5:c.*1035A>G | ENSP00000420253.1:p.= | |
| ENST00000493795.5:c.958A>G | ENSP00000418775.1:p.Thr320Ala | |
| ENST00000493919.5:c.646+312A>G | ENSP00000418819.1:p.= | |
| ENST00000494123.5:c.1099A>G | ENSP00000419103.1:p.Thr367Ala | |
| ENST00000497488.1:c.211A>G | ENSP00000418986.1:p.Thr71Ala | |
| ENST00000586385.5:c.5-30481A>G | ENSP00000465818.1:p.= | |
| ENST00000591534.5:c.-43-19911A>G | ENSP00000467329.1:p.= | |
| ENST00000591849.5:c.-99+30839A>G | ENSP00000465347.1:p.= | |
| ENST00000634433.1:c.976A>G | ENSP00000489431.1:p.Thr326Ala |