Linked Data
ClinVar Variation Id:
2934568
ClinVar RCV Id:
RCV003798270
MyVariant Identifiers:
chr3:g.33110381C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33068889C>G , CM000665.2:g.33068889C>G | GRCh38 |
| NC_000003.11:g.33110381C>G , CM000665.1:g.33110381C>G | GRCh37 |
| NC_000003.10:g.33085385C>G | NCBI36 |
| NG_009005.1:g.33314G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.327G>C MANE Select | ENSP00000306920.4:p.Arg109= | |
| ENST00000307363.9:c.327G>C | ENSP00000306920.4:p.Arg109= | |
| ENST00000307377.12:c.246-3332G>C | ENSP00000305920.8:n.246-3332G>C | |
| ENST00000399402.7:c.237G>C | ENSP00000382333.2:p.Arg79= | |
| ENST00000415454.1:c.76-10620G>C | ENSP00000411813.1:n.76-10620G>C | |
| ENST00000438227.1:c.76-3332G>C | ENSP00000401250.1:n.76-3332G>C | |
| ENST00000440656.1:c.-67G>C | ENSP00000411769.1:n.-67G>C | |
| ENST00000446732.5:c.156-3332G>C | ENSP00000407365.1:n.156-3332G>C | |
| ENST00000450835.1:c.237G>C | ENSP00000403264.1:p.Arg79= | |
| ENST00000464355.1:n.285G>C | ||
| ENST00000482097.5:n.109-15340G>C | ||
| ENST00000485698.5:n.137-15340G>C | ||
| ENST00000498537.5:n.133-15340G>C | ||
| NM_000404.2:c.327G>C | NP_000395.2:p.Arg109= | |
| NM_000404.3:c.327G>C | NP_000395.2:p.Arg109= | |
| NM_001079811.1:c.237G>C | NP_001073279.1:p.Arg79= | |
| NM_001079811.2:c.237G>C | NP_001073279.1:p.Arg79= | |
| NM_001135602.1:c.246-3332G>C | NP_001129074.1:n.246-3332G>C | |
| NM_001135602.2:c.246-3332G>C | NP_001129074.1:n.246-3332G>C | |
| NM_001317040.1:c.471G>C | NP_001303969.1:p.Arg157= | |
| NM_000404.4:c.327G>C MANE Select | NP_000395.3:p.Arg109= | |
| NM_001079811.3:c.237G>C | NP_001073279.2:p.Arg79= | |
| NM_001135602.3:c.246-3332G>C | NP_001129074.2:n.246-3332G>C | |
| NM_001317040.2:c.471G>C | NP_001303969.2:p.Arg157= | |
| NM_001393580.1:c.327G>C | NP_001380509.1:p.Arg109= |