Linked Data
ClinVar Variation Id:
288385
dbSNP Id:
rs763395740
ExAC:
2:238249200 C / T
gnomAD v2:
2-238249200-C-T
gnomAD v3:
2-237340557-C-T
gnomAD v4:
2-237340557-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237340557C>T , CM000664.2:g.237340557C>T | GRCh38 |
| NC_000002.11:g.238249200C>T , CM000664.1:g.238249200C>T | GRCh37 |
| NC_000002.10:g.237913939C>T | NCBI36 |
| NG_008676.1:g.78651G>A , LRG_473:g.78651G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000347401.8:c.1004G>A | ||
| ENST00000353578.9:c.7741G>A | ENSP00000315873.4:p.Ala2581Thr | |
| ENST00000682957.1:c.362G>A | ||
| ENST00000684508.1:n.626G>A | ||
| ENST00000295550.9:c.8359G>A MANE Select | ENSP00000295550.4:p.Ala2787Thr | |
| ENST00000295550.8:c.8359G>A | ENSP00000295550.4:p.Ala2787Thr | |
| ENST00000347401.7:c.6535G>A | ENSP00000315609.4:p.Ala2179Thr | |
| ENST00000353578.8:c.7741G>A | ENSP00000315873.4:p.Ala2581Thr | |
| ENST00000409809.5:c.7741G>A | ENSP00000386844.1:p.Ala2581Thr | |
| ENST00000468792.1:n.46G>A | ||
| ENST00000472056.5:c.6538G>A | ENSP00000418285.1:p.Ala2180Thr | |
| ENST00000491769.1:n.4801G>A | ||
| NM_004369.3:c.8359G>A , LRG_473t1:c.8359G>A | NP_004360.2:p.Ala2787Thr | |
| NM_057166.4:c.6538G>A | NP_476507.3:p.Ala2180Thr | |
| NM_057167.3:c.7741G>A | NP_476508.2:p.Ala2581Thr | |
| XM_005246065.1:c.7759G>A | XP_005246122.1:p.Ala2587Thr | |
| XM_005246066.1:c.7138G>A | XP_005246123.1:p.Ala2380Thr | |
| XM_006712253.1:c.7858G>A | XP_006712316.1:p.Ala2620Thr | |
| XM_011510574.1:c.8356G>A | XP_011508876.1:p.Ala2786Thr | |
| XM_011510575.1:c.5953G>A | XP_011508877.1:p.Ala1985Thr | |
| XM_017003304.1:c.5953G>A | XP_016858793.1:p.Ala1985Thr | |
| XM_024452684.1:c.7138G>A | XP_024308452.1:p.Ala2380Thr | |
| NM_004369.4:c.8359G>A MANE Select | NP_004360.2:p.Ala2787Thr | |
| NM_057166.5:c.6538G>A | NP_476507.3:p.Ala2180Thr | |
| NM_057167.4:c.7741G>A | NP_476508.2:p.Ala2581Thr |