Linked Data
ClinVar Variation Id:
2652038
ClinVar RCV Id:
RCV003440251
MyVariant Identifiers:
chr2:g.238245091G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237336448G>A , CM000664.2:g.237336448G>A | GRCh38 |
| NC_000002.11:g.238245091G>A , CM000664.1:g.238245091G>A | GRCh37 |
| NC_000002.10:g.237909830G>A | NCBI36 |
| NG_008676.1:g.82760C>T , LRG_473:g.82760C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347401.8:c.1297C>T | ||
| ENST00000353578.9:c.8034C>T | ENSP00000315873.4:p.Thr2678= | |
| ENST00000682957.1:c.779C>T | ||
| ENST00000684508.1:n.919C>T | ||
| ENST00000295550.9:c.8652C>T MANE Select | ENSP00000295550.4:p.Thr2884= | |
| ENST00000295550.8:c.8652C>T | ENSP00000295550.4:p.Thr2884= | |
| ENST00000347401.7:c.6828C>T | ENSP00000315609.4:p.Thr2276= | |
| ENST00000353578.8:c.8034C>T | ENSP00000315873.4:p.Thr2678= | |
| ENST00000409809.5:c.8034C>T | ENSP00000386844.1:p.Thr2678= | |
| ENST00000472056.5:c.6831C>T | ENSP00000418285.1:p.Thr2277= | |
| ENST00000491769.1:n.5094C>T | ||
| NM_004369.3:c.8652C>T , LRG_473t1:c.8652C>T | NP_004360.2:p.Thr2884= | |
| NM_057166.4:c.6831C>T | NP_476507.3:p.Thr2277= | |
| NM_057167.3:c.8034C>T | NP_476508.2:p.Thr2678= | |
| XM_005246065.1:c.8052C>T | XP_005246122.1:p.Thr2684= | |
| XM_005246066.1:c.7431C>T | XP_005246123.1:p.Thr2477= | |
| XM_006712253.1:c.8151C>T | XP_006712316.1:p.Thr2717= | |
| XM_011510574.1:c.8649C>T | XP_011508876.1:p.Thr2883= | |
| XM_011510575.1:c.6246C>T | XP_011508877.1:p.Thr2082= | |
| XM_017003304.1:c.6246C>T | XP_016858793.1:p.Thr2082= | |
| XM_024452684.1:c.7431C>T | XP_024308452.1:p.Thr2477= | |
| NM_004369.4:c.8652C>T MANE Select | NP_004360.2:p.Thr2884= | |
| NM_057166.5:c.6831C>T | NP_476507.3:p.Thr2277= | |
| NM_057167.4:c.8034C>T | NP_476508.2:p.Thr2678= |