Linked Data
ClinVar Variation Id:
2936379
ClinVar RCV Id:
RCV003796665
MyVariant Identifiers:
chr4:g.5620297G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5618570G>T , CM000666.2:g.5618570G>T | GRCh38 |
| NC_000004.11:g.5620297G>T , CM000666.1:g.5620297G>T | GRCh37 |
| NC_000004.10:g.5671198G>T | NCBI36 |
| NG_015821.1:g.95979C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344408.10:c.2614C>A MANE Select | ENSP00000342144.5:p.Arg872= | |
| ENST00000310917.6:c.2374C>A | ENSP00000311683.2:p.Arg792= | |
| ENST00000344408.9:c.2614C>A | ENSP00000342144.5:p.Arg872= | |
| ENST00000475313.5:c.2374C>A | ENSP00000431981.1:p.Arg792= | |
| ENST00000509670.1:c.*1007C>A | ENSP00000423876.1:n.*1007C>A | |
| NM_001166136.1:c.2374C>A | NP_001159608.1:p.Arg792= | |
| NM_147127.4:c.2614C>A | NP_667338.3:p.Arg872= | |
| XM_011513392.1:c.2623C>A | XP_011511694.1:p.Arg875= | |
| XM_011513393.1:c.2623C>A | XP_011511695.1:p.Arg875= | |
| XM_011513394.1:c.2383C>A | XP_011511696.1:p.Arg795= | |
| XM_017007736.1:c.2374C>A | XP_016863225.1:p.Arg792= | |
| XM_017007737.1:c.2374C>A | XP_016863226.1:p.Arg792= | |
| XM_017007738.1:c.2614C>A | XP_016863227.1:p.Arg872= | |
| XM_017007739.1:c.934C>A | XP_016863228.1:p.Arg312= | |
| XM_024453893.1:c.934C>A | XP_024309661.1:p.Arg312= | |
| XR_001741141.1:n.2679C>A | ||
| NM_147127.5:c.2614C>A MANE Select | NP_667338.3:p.Arg872= | |
| NM_001166136.2:c.2374C>A | NP_001159608.1:p.Arg792= |