Linked Data
ClinVar Variation Id:
343937
dbSNP Id:
rs149049400
ExAC:
3:158409190 C / T
gnomAD v2:
3-158409190-C-T
gnomAD v3:
3-158691401-C-T
gnomAD v4:
3-158691401-C-T
COSMIC:
COSM266582
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.158691401C>T , CM000665.2:g.158691401C>T | GRCh38 |
| NC_000003.11:g.158409190C>T , CM000665.1:g.158409190C>T | GRCh37 |
| NC_000003.10:g.159891884C>T | NCBI36 |
| NG_008441.1:g.51874C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000486715.6:c.2190C>T MANE Select | ENSP00000419038.1:p.Asp730= | |
| ENST00000264263.9:c.2247C>T | ENSP00000264263.5:p.Asp749= | |
| ENST00000472383.1:c.158C>T | ||
| ENST00000478254.5:c.*830C>T | ENSP00000417225.1:n.*830C>T | |
| ENST00000486715.5:c.2190C>T | ENSP00000419038.1:p.Asp730= | |
| NM_001308164.1:c.2247C>T | NP_001295093.1:p.Asp749= | |
| NM_024996.5:c.2190C>T | NP_079272.4:p.Asp730= | |
| XM_006713795.1:c.2073C>T | XP_006713858.1:p.Asp691= | |
| XM_006713795.2:c.2073C>T | XP_006713858.1:p.Asp691= | |
| NM_001374355.1:c.2109C>T | NP_001361284.1:p.Asp703= | |
| NM_001374356.1:c.2073C>T | NP_001361285.1:p.Asp691= | |
| NM_001374357.1:c.1965C>T | NP_001361286.1:p.Asp655= | |
| NM_001374358.1:c.1731C>T | NP_001361287.1:p.Asp577= | |
| NM_001374359.1:c.1623C>T | NP_001361288.1:p.Asp541= | |
| NM_001374360.1:c.1569C>T | NP_001361289.1:p.Asp523= | |
| NM_001374361.1:c.1506C>T | NP_001361290.1:p.Asp502= | |
| NM_024996.7:c.2190C>T MANE Select | NP_079272.4:p.Asp730= | |
| NR_164499.1:n.2213C>T | ||
| NR_164500.1:n.2153C>T | ||
| NR_164501.1:n.1698C>T | ||
| NR_164502.1:n.2177C>T | ||
| NM_001308164.2:c.2247C>T | NP_001295093.1:p.Asp749= |