Linked Data
ClinVar Variation Id:
950215
ClinVar RCV Id:
RCV001221882
dbSNP Id:
rs1443654986
gnomAD v3:
17-58692664-C-G
gnomAD v4:
17-58692664-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58692664C>G , CM000679.2:g.58692664C>G | GRCh38 |
| NC_000017.10:g.56770025C>G , CM000679.1:g.56770025C>G | GRCh37 |
| NC_000017.9:g.54125024C>G | NCBI36 |
| NG_023199.1:g.5063C>G , LRG_314:g.5063C>G | |
| NG_047169.1:g.4416G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461271.6:c.-228C>G | ENSP00000464056.2:n.-228C>G | |
| ENST00000697675.1:n.92C>G | ||
| ENST00000697676.1:n.81C>G | ||
| ENST00000697677.1:n.79C>G | ||
| ENST00000697678.1:n.47+32C>G | ||
| ENST00000697679.1:n.72C>G | ||
| ENST00000697680.1:c.21C>G | ENSP00000513392.1:p.Arg7= | |
| ENST00000697681.1:c.21C>G | ENSP00000513393.1:p.Arg7= | |
| ENST00000697683.1:c.21C>G | ENSP00000513395.1:p.Arg7= | |
| ENST00000697684.1:n.81C>G | ||
| ENST00000697685.1:c.21C>G | ENSP00000513396.1:p.Arg7= | |
| ENST00000697686.1:c.-207+32C>G | ENSP00000513397.1:n.-207+32C>G | |
| ENST00000697687.1:n.67C>G | ||
| ENST00000697688.1:n.67C>G | ||
| ENST00000697689.1:c.21C>G | ENSP00000513398.1:p.Arg7= | |
| ENST00000697690.1:c.21C>G | ENSP00000513399.1:p.Arg7= | |
| ENST00000697691.1:c.21C>G | ENSP00000513400.1:p.Arg7= | |
| ENST00000697692.1:c.21C>G | ENSP00000513401.1:p.Arg7= | |
| ENST00000337432.9:c.21C>G MANE Select | ENSP00000336701.4:p.Arg7= | |
| ENST00000337432.8:c.21C>G | ENSP00000336701.4:p.Arg7= | |
| ENST00000421782.3:c.21C>G | ENSP00000391450.2:p.Arg7= | |
| ENST00000461271.5:c.-228C>G | ENSP00000464056.1:n.-228C>G | |
| ENST00000475762.5:c.21C>G | ENSP00000432421.1:p.Arg7= | |
| ENST00000476741.2:n.63C>G | ||
| ENST00000482007.5:c.21C>G | ENSP00000433332.1:p.Arg7= | |
| ENST00000486827.1:c.21C>G | ENSP00000436761.1:p.Arg7= | |
| ENST00000487525.5:c.21C>G | ENSP00000431637.1:p.Arg7= | |
| ENST00000487921.5:n.57+32C>G | ||
| ENST00000583539.5:c.21C>G | ENSP00000463121.1:p.Arg7= | |
| ENST00000584617.5:c.2C>G | ||
| NM_002876.3:c.21C>G | NP_002867.1:p.Arg7= | |
| NM_058216.2:c.21C>G | NP_478123.1:p.Arg7= | |
| NR_103872.1:n.92C>G | ||
| NR_103873.1:n.92C>G | ||
| XM_006722001.2:c.21C>G | XP_006722064.1:p.Arg7= | |
| XM_006722002.2:c.21C>G | XP_006722065.1:p.Arg7= | |
| XM_006722004.2:c.-228C>G | XP_006722067.1:n.-228C>G | |
| XM_006722005.2:c.-207+32C>G | XP_006722068.1:n.-207+32C>G | |
| XM_011525092.1:c.-528C>G | XP_011523394.1:n.-528C>G | |
| XM_011525093.1:c.-689C>G | XP_011523395.1:n.-689C>G | |
| XR_934513.1:n.94C>G | ||
| XR_934514.1:n.94C>G | ||
| XM_006722001.4:c.21C>G | XP_006722064.1:p.Arg7= | |
| XM_006722002.4:c.21C>G | XP_006722065.1:p.Arg7= | |
| XM_006722004.3:c.-228C>G | XP_006722067.1:n.-228C>G | |
| XM_006722005.3:c.-207+32C>G | XP_006722068.1:n.-207+32C>G | |
| XM_017024914.1:c.-228C>G | XP_016880403.1:n.-228C>G | |
| XM_017024916.1:c.-528C>G | XP_016880405.1:n.-528C>G | |
| XM_017024917.1:c.-207+32C>G | XP_016880406.1:n.-207+32C>G | |
| XM_017024918.2:c.-502C>G | XP_016880407.1:n.-502C>G | |
| XR_934513.3:n.525C>G | ||
| XR_934514.3:n.525C>G | ||
| NM_058216.3:c.21C>G MANE Select | NP_478123.1:p.Arg7= | |
| NR_103872.2:n.63C>G | ||
| NM_002876.4:c.21C>G | NP_002867.1:p.Arg7= |