Linked Data
ClinVar Variation Id:
282135
dbSNP Id:
rs764225803
ExAC:
2:238277444 G / A
gnomAD v2:
2-238277444-G-A
gnomAD v3:
2-237368801-G-A
gnomAD v4:
2-237368801-G-A
COSMIC:
COSM5006312
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237368801G>A , CM000664.2:g.237368801G>A | GRCh38 |
| NC_000002.11:g.238277444G>A , CM000664.1:g.238277444G>A | GRCh37 |
| NC_000002.10:g.237942183G>A | NCBI36 |
| NG_008676.1:g.50407C>T , LRG_473:g.50407C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000353578.9:c.4044C>T | ENSP00000315873.4:p.Asp1348= | |
| ENST00000684597.1:c.117-125C>T | ||
| ENST00000295550.9:c.4662C>T MANE Select | ENSP00000295550.4:p.Asp1554= | |
| ENST00000295550.8:c.4662C>T | ENSP00000295550.4:p.Asp1554= | |
| ENST00000347401.7:c.2841C>T | ENSP00000315609.4:p.Asp947= | |
| ENST00000353578.8:c.4044C>T | ENSP00000315873.4:p.Asp1348= | |
| ENST00000409809.5:c.4044C>T | ENSP00000386844.1:p.Asp1348= | |
| ENST00000472056.5:c.2841C>T | ENSP00000418285.1:p.Asp947= | |
| NM_004369.3:c.4662C>T , LRG_473t1:c.4662C>T | NP_004360.2:p.Asp1554= | |
| NM_057166.4:c.2841C>T | NP_476507.3:p.Asp947= | |
| NM_057167.3:c.4044C>T | NP_476508.2:p.Asp1348= | |
| XM_005246065.1:c.4062C>T | XP_005246122.1:p.Asp1354= | |
| XM_005246066.1:c.3441C>T | XP_005246123.1:p.Asp1147= | |
| XM_006712253.1:c.4286-125C>T | XP_006712316.1:n.4286-125C>T | |
| XM_011510574.1:c.4659C>T | XP_011508876.1:p.Asp1553= | |
| XM_011510575.1:c.2256C>T | XP_011508877.1:p.Asp752= | |
| XM_017003304.1:c.2256C>T | XP_016858793.1:p.Asp752= | |
| XM_024452684.1:c.3441C>T | XP_024308452.1:p.Asp1147= | |
| NM_004369.4:c.4662C>T MANE Select | NP_004360.2:p.Asp1554= | |
| NM_057166.5:c.2841C>T | NP_476507.3:p.Asp947= | |
| NM_057167.4:c.4044C>T | NP_476508.2:p.Asp1348= |