Linked Data
ClinVar Variation Id:
215088
dbSNP Id:
rs147315735
ExAC:
8:103236280 T / C
gnomAD v2:
8-103236280-T-C
gnomAD v3:
8-102224052-T-C
gnomAD v4:
8-102224052-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.102224052T>C , CM000670.2:g.102224052T>C | GRCh38 |
| NC_000008.10:g.103236280T>C , CM000670.1:g.103236280T>C | GRCh37 |
| NC_000008.9:g.103305456T>C | NCBI36 |
| NG_016617.1:g.20067A>G , LRG_788:g.20067A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251810.8:c.544A>G MANE Select | ENSP00000251810.3:p.Thr182Ala | |
| ENST00000251810.7:c.544A>G | ENSP00000251810.3:p.Thr182Ala | |
| ENST00000395912.6:c.388A>G | ENSP00000379248.2:p.Thr130Ala | |
| ENST00000519317.5:c.49-9894A>G | ENSP00000430641.1:n.49-9894A>G | |
| ENST00000519962.5:c.48+14775A>G | ENSP00000429140.1:n.48+14775A>G | |
| ENST00000522368.5:c.713A>G | ||
| ENST00000522394.1:c.122+8179A>G | ENSP00000429578.1:n.122+8179A>G | |
| ENST00000621845.1:c.382A>G | ENSP00000484318.1:p.Thr128Ala | |
| NM_001172477.1:c.760A>G , LRG_788t1:c.760A>G | NP_001165948.1:p.Thr254Ala | |
| NM_001172478.1:c.388A>G | NP_001165949.1:p.Thr130Ala | |
| NM_015713.4:c.544A>G , LRG_788t2:c.544A>G | NP_056528.2:p.Thr182Ala | |
| NM_001172478.2:c.388A>G | NP_001165949.1:p.Thr130Ala | |
| NM_015713.5:c.544A>G MANE Select | NP_056528.2:p.Thr182Ala |