Linked Data
ClinVar Variation Id:
292983
dbSNP Id:
rs201910178
ExAC:
1:158612645 T / C
gnomAD v2:
1-158612645-T-C
gnomAD v3:
1-158642855-T-C
gnomAD v4:
1-158642855-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.158642855T>C , CM000663.2:g.158642855T>C | GRCh38 |
| NC_000001.10:g.158612645T>C , CM000663.1:g.158612645T>C | GRCh37 |
| NC_000001.9:g.156879269T>C | NCBI36 |
| NG_011474.1:g.48862A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643759.2:c.4564A>G MANE Select | ENSP00000495214.1:p.Thr1522Ala | |
| ENST00000368147.8:c.4564A>G | ENSP00000357129.4:p.Thr1522Ala | |
| ENST00000614909.4:c.4564A>G | ENSP00000482595.1:p.Thr1522Ala | |
| NM_003126.2:c.4564A>G | NP_003117.2:p.Thr1522Ala | |
| XM_011509916.1:c.4564A>G | XP_011508218.1:p.Thr1522Ala | |
| XM_011509917.1:c.4564A>G | XP_011508219.1:p.Thr1522Ala | |
| XM_011509918.1:c.4564A>G | XP_011508220.1:p.Thr1522Ala | |
| XM_011509919.1:c.4564A>G | XP_011508221.1:p.Thr1522Ala | |
| XR_921911.1:n.4677A>G | ||
| XR_921912.1:n.4752A>G | ||
| NM_003126.3:c.4564A>G | NP_003117.2:p.Thr1522Ala | |
| XM_011509916.2:c.4564A>G | XP_011508218.1:p.Thr1522Ala | |
| XM_011509917.3:c.4564A>G | XP_011508219.1:p.Thr1522Ala | |
| XM_011509918.3:c.4564A>G | XP_011508220.1:p.Thr1522Ala | |
| XM_011509919.3:c.4564A>G | XP_011508221.1:p.Thr1522Ala | |
| XR_921911.3:n.4690A>G | ||
| XR_921912.2:n.4762A>G | ||
| NM_003126.4:c.4564A>G MANE Select | NP_003117.2:p.Thr1522Ala |