Linked Data
ClinVar Variation Id:
288872
dbSNP Id:
rs372154635
ExAC:
2:238259820 C / T
gnomAD v2:
2-238259820-C-T
gnomAD v3:
2-237351177-C-T
gnomAD v4:
2-237351177-C-T
COSMIC:
COSM1565670
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237351177C>T , CM000664.2:g.237351177C>T | GRCh38 |
| NC_000002.11:g.238259820C>T , CM000664.1:g.238259820C>T | GRCh37 |
| NC_000002.10:g.237924559C>T | NCBI36 |
| NG_008676.1:g.68031G>A , LRG_473:g.68031G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000353578.9:c.6151G>A | ENSP00000315873.4:p.Ala2051Thr | |
| ENST00000295550.9:c.6769G>A MANE Select | ENSP00000295550.4:p.Ala2257Thr | |
| ENST00000295550.8:c.6769G>A | ENSP00000295550.4:p.Ala2257Thr | |
| ENST00000347401.7:c.4948G>A | ENSP00000315609.4:p.Ala1650Thr | |
| ENST00000353578.8:c.6151G>A | ENSP00000315873.4:p.Ala2051Thr | |
| ENST00000409809.5:c.6151G>A | ENSP00000386844.1:p.Ala2051Thr | |
| ENST00000472056.5:c.4948G>A | ENSP00000418285.1:p.Ala1650Thr | |
| ENST00000491769.1:n.1023G>A | ||
| NM_004369.3:c.6769G>A , LRG_473t1:c.6769G>A | NP_004360.2:p.Ala2257Thr | |
| NM_057166.4:c.4948G>A | NP_476507.3:p.Ala1650Thr | |
| NM_057167.3:c.6151G>A | NP_476508.2:p.Ala2051Thr | |
| XM_005246065.1:c.6169G>A | XP_005246122.1:p.Ala2057Thr | |
| XM_005246066.1:c.5548G>A | XP_005246123.1:p.Ala1850Thr | |
| XM_006712253.1:c.6268G>A | XP_006712316.1:p.Ala2090Thr | |
| XM_011510574.1:c.6766G>A | XP_011508876.1:p.Ala2256Thr | |
| XM_011510575.1:c.4363G>A | XP_011508877.1:p.Ala1455Thr | |
| XM_017003304.1:c.4363G>A | XP_016858793.1:p.Ala1455Thr | |
| XM_024452684.1:c.5548G>A | XP_024308452.1:p.Ala1850Thr | |
| NM_004369.4:c.6769G>A MANE Select | NP_004360.2:p.Ala2257Thr | |
| NM_057166.5:c.4948G>A | NP_476507.3:p.Ala1650Thr | |
| NM_057167.4:c.6151G>A | NP_476508.2:p.Ala2051Thr |