Linked Data
dbSNP Id:
rs767416852
ExAC:
2:238245066 T / C
gnomAD v2:
2-238245066-T-C
gnomAD v4:
2-237336423-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237336423T>C , CM000664.2:g.237336423T>C | GRCh38 |
| NC_000002.11:g.238245066T>C , CM000664.1:g.238245066T>C | GRCh37 |
| NC_000002.10:g.237909805T>C | NCBI36 |
| NG_008676.1:g.82785A>G , LRG_473:g.82785A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347401.8:c.1322A>G | ||
| ENST00000353578.9:c.8059A>G | ENSP00000315873.4:p.Thr2687Ala | |
| ENST00000682957.1:c.804A>G | ||
| ENST00000684508.1:n.944A>G | ||
| ENST00000295550.9:c.8677A>G MANE Select | ENSP00000295550.4:p.Thr2893Ala | |
| ENST00000295550.8:c.8677A>G | ENSP00000295550.4:p.Thr2893Ala | |
| ENST00000347401.7:c.6853A>G | ENSP00000315609.4:p.Thr2285Ala | |
| ENST00000353578.8:c.8059A>G | ENSP00000315873.4:p.Thr2687Ala | |
| ENST00000409809.5:c.8059A>G | ENSP00000386844.1:p.Thr2687Ala | |
| ENST00000472056.5:c.6856A>G | ENSP00000418285.1:p.Thr2286Ala | |
| ENST00000491769.1:n.5119A>G | ||
| NM_004369.3:c.8677A>G , LRG_473t1:c.8677A>G | NP_004360.2:p.Thr2893Ala | |
| NM_057166.4:c.6856A>G | NP_476507.3:p.Thr2286Ala | |
| NM_057167.3:c.8059A>G | NP_476508.2:p.Thr2687Ala | |
| XM_005246065.1:c.8077A>G | XP_005246122.1:p.Thr2693Ala | |
| XM_005246066.1:c.7456A>G | XP_005246123.1:p.Thr2486Ala | |
| XM_006712253.1:c.8176A>G | XP_006712316.1:p.Thr2726Ala | |
| XM_011510574.1:c.8674A>G | XP_011508876.1:p.Thr2892Ala | |
| XM_011510575.1:c.6271A>G | XP_011508877.1:p.Thr2091Ala | |
| XM_017003304.1:c.6271A>G | XP_016858793.1:p.Thr2091Ala | |
| XM_024452684.1:c.7456A>G | XP_024308452.1:p.Thr2486Ala | |
| NM_004369.4:c.8677A>G MANE Select | NP_004360.2:p.Thr2893Ala | |
| NM_057166.5:c.6856A>G | NP_476507.3:p.Thr2286Ala | |
| NM_057167.4:c.8059A>G | NP_476508.2:p.Thr2687Ala |