Linked Data
ClinVar Variation Id:
2935388
ClinVar RCV Id:
RCV003791042
dbSNP Id:
rs576455064
ExAC:
4:5620378 C / A
gnomAD v2:
4-5620378-C-A
gnomAD v4:
4-5618651-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5618651C>A , CM000666.2:g.5618651C>A | GRCh38 |
| NC_000004.11:g.5620378C>A , CM000666.1:g.5620378C>A | GRCh37 |
| NC_000004.10:g.5671279C>A | NCBI36 |
| NG_015821.1:g.95898G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344408.10:c.2533G>T MANE Select | ENSP00000342144.5:p.Glu845Ter | |
| ENST00000310917.6:c.2293G>T | ENSP00000311683.2:p.Glu765Ter | |
| ENST00000344408.9:c.2533G>T | ENSP00000342144.5:p.Glu845Ter | |
| ENST00000475313.5:c.2293G>T | ENSP00000431981.1:p.Glu765Ter | |
| ENST00000509670.1:c.*926G>T | ENSP00000423876.1:n.*926G>T | |
| NM_001166136.1:c.2293G>T | NP_001159608.1:p.Glu765Ter | |
| NM_147127.4:c.2533G>T | NP_667338.3:p.Glu845Ter | |
| XM_011513392.1:c.2542G>T | XP_011511694.1:p.Glu848Ter | |
| XM_011513393.1:c.2542G>T | XP_011511695.1:p.Glu848Ter | |
| XM_011513394.1:c.2302G>T | XP_011511696.1:p.Glu768Ter | |
| XM_017007736.1:c.2293G>T | XP_016863225.1:p.Glu765Ter | |
| XM_017007737.1:c.2293G>T | XP_016863226.1:p.Glu765Ter | |
| XM_017007738.1:c.2533G>T | XP_016863227.1:p.Glu845Ter | |
| XM_017007739.1:c.853G>T | XP_016863228.1:p.Glu285Ter | |
| XM_024453893.1:c.853G>T | XP_024309661.1:p.Glu285Ter | |
| XR_001741141.1:n.2598G>T | ||
| NM_147127.5:c.2533G>T MANE Select | NP_667338.3:p.Glu845Ter | |
| NM_001166136.2:c.2293G>T | NP_001159608.1:p.Glu765Ter |