Linked Data
ClinVar Variation Id:
293838
ClinVar RCV Id:
RCV000349816
dbSNP Id:
rs192187532
ExAC:
1:173878838 C / T
gnomAD v2:
1-173878838-C-T
gnomAD v3:
1-173909700-C-T
gnomAD v4:
1-173909700-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173909700C>T , CM000663.2:g.173909700C>T | GRCh38 |
| NC_000001.10:g.173878838C>T , CM000663.1:g.173878838C>T | GRCh37 |
| NC_000001.9:g.172145461C>T | NCBI36 |
| NG_012462.1:g.12679G>A , LRG_577:g.12679G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.1005G>A MANE Select | ENSP00000356671.3:p.Val335= | |
| ENST00000367698.3:c.1005G>A | ENSP00000356671.3:p.Val335= | |
| ENST00000617423.4:c.559+2164G>A | ENSP00000478688.1:n.559+2164G>A | |
| NM_000488.3:c.1005G>A , LRG_577t1:c.1005G>A | NP_000479.1:p.Val335= | |
| XM_005245198.2:c.861G>A | XP_005245255.1:p.Val287= | |
| NM_001365052.1:c.861G>A | NP_001351981.1:p.Val287= | |
| NM_000488.4:c.1005G>A MANE Select | NP_000479.1:p.Val335= | |
| NM_001365052.2:c.861G>A | NP_001351981.1:p.Val287= | |
| NM_001386302.1:c.1128G>A | NP_001373231.1:p.Val376= | |
| NM_001386303.1:c.1086G>A | NP_001373232.1:p.Val362= | |
| NM_001386304.1:c.984G>A | NP_001373233.1:p.Val328= | |
| NM_001386305.1:c.948G>A | NP_001373234.1:p.Val316= | |
| NM_001386306.1:c.789G>A | NP_001373235.1:p.Val263= |