Linked Data
ClinVar Variation Id:
392495
dbSNP Id:
rs779449573
ExAC:
2:32288919 C / A
gnomAD v2:
2-32288919-C-A
gnomAD v4:
2-32063850-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.32063850C>A , CM000664.2:g.32063850C>A | GRCh38 |
| NC_000002.11:g.32288919C>A , CM000664.1:g.32288919C>A | GRCh37 |
| NC_000002.10:g.32142423C>A | NCBI36 |
| NG_008730.1:g.5240C>A , LRG_714:g.5240C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704289.1:c.19C>A | ENSP00000515816.1:p.Arg7= | |
| ENST00000315285.9:c.19C>A MANE Select | ENSP00000320885.3:p.Arg7= | |
| ENST00000621856.2:c.19C>A | ENSP00000482496.2:p.Arg7= | |
| ENST00000642455.1:c.19C>A | ENSP00000493827.1:p.Arg7= | |
| ENST00000646571.1:c.19C>A | ENSP00000495015.1:p.Arg7= | |
| ENST00000315285.7:c.19C>A | ENSP00000320885.3:p.Arg7= | |
| ENST00000345662.5:c.19C>A | ENSP00000340817.1:p.Arg7= | |
| ENST00000615843.4:c.19C>A | ENSP00000480893.1:p.Arg7= | |
| NM_014946.3:c.19C>A , LRG_714t1:c.19C>A | NP_055761.2:p.Arg7= | |
| NM_199436.1:c.19C>A | NP_955468.1:p.Arg7= | |
| XM_005264516.3:c.19C>A | XP_005264573.1:p.Arg7= | |
| XM_011533067.1:c.19C>A | XP_011531369.1:p.Arg7= | |
| NM_001363823.1:c.19C>A | NP_001350752.1:p.Arg7= | |
| NM_001363875.1:c.19C>A | NP_001350804.1:p.Arg7= | |
| XM_005264516.5:c.19C>A | XP_005264573.1:p.Arg7= | |
| XM_011533067.2:c.19C>A | XP_011531369.1:p.Arg7= | |
| XM_017004778.2:c.19C>A | XP_016860267.1:p.Arg7= | |
| NM_001363823.2:c.19C>A | NP_001350752.1:p.Arg7= | |
| NM_001363875.2:c.19C>A | NP_001350804.1:p.Arg7= | |
| NM_001377959.1:c.19C>A | NP_001364888.1:p.Arg7= | |
| NM_014946.4:c.19C>A MANE Select | NP_055761.2:p.Arg7= | |
| NM_199436.2:c.19C>A | NP_955468.1:p.Arg7= |