Linked Data
ClinVar Variation Id:
1114059
ClinVar RCV Id:
RCV001441608
dbSNP Id:
rs2108003859
MyVariant Identifiers:
chr3:g.158364704C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.158646915C>T , CM000665.2:g.158646915C>T | GRCh38 |
| NC_000003.11:g.158364704C>T , CM000665.1:g.158364704C>T | GRCh37 |
| NC_000003.10:g.159847398C>T | NCBI36 |
| NG_008441.1:g.7388C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000486715.6:c.540C>T (GFM1) MANE Select | ENSP00000419038.1:p.Gly180= | |
| ENST00000264263.9:c.540C>T (GFM1) | ENSP00000264263.5:p.Gly180= | |
| ENST00000478251.1:n.28C>T (GFM1) | ||
| ENST00000478254.5:c.540C>T (GFM1) | ENSP00000417225.1:p.Gly180= | |
| ENST00000478576.5:c.540C>T (GFM1) | ENSP00000418755.1:p.Gly180= | |
| ENST00000482640.5:c.362-706G>A (LXN) | ||
| ENST00000486715.5:c.540C>T (GFM1) | ENSP00000419038.1:p.Gly180= | |
| NM_001308164.1:c.540C>T (GFM1) | NP_001295093.1:p.Gly180= | |
| NM_001308166.1:c.540C>T (GFM1) | NP_001295095.1:p.Gly180= | |
| NM_024996.5:c.540C>T (GFM1) | NP_079272.4:p.Gly180= | |
| XM_006713795.1:c.540C>T (GFM1) | XP_006713858.1:p.Gly180= | |
| XM_006713795.2:c.540C>T (GFM1) | XP_006713858.1:p.Gly180= | |
| NM_001374355.1:c.540C>T (GFM1) | NP_001361284.1:p.Gly180= | |
| NM_001374356.1:c.540C>T (GFM1) | NP_001361285.1:p.Gly180= | |
| NM_001374357.1:c.315C>T (GFM1) | NP_001361286.1:p.Gly105= | |
| NM_001374358.1:c.234+1134C>T (GFM1) | NP_001361287.1:n.234+1134C>T | |
| NM_001374359.1:c.5+1134C>T (GFM1) | NP_001361288.1:n.5+1134C>T | |
| NM_001374360.1:c.5+1134C>T (GFM1) | NP_001361289.1:n.5+1134C>T | |
| NM_001374361.1:c.5+1134C>T (GFM1) | NP_001361290.1:n.5+1134C>T | |
| NM_024996.7:c.540C>T (GFM1) MANE Select | NP_079272.4:p.Gly180= | |
| NR_164499.1:n.648C>T (GFM1) | ||
| NR_164500.1:n.648C>T (GFM1) | ||
| NR_164501.1:n.342+1134C>T (GFM1) | ||
| NR_164502.1:n.648C>T (GFM1) | ||
| NM_001308164.2:c.540C>T (GFM1) | NP_001295093.1:p.Gly180= | |
| NM_001308166.2:c.540C>T (GFM1) | NP_001295095.1:p.Gly180= |