Linked Data
ClinVar Variation Id:
2073159
ClinVar RCV Id:
RCV002971668
dbSNP Id:
rs1411024903
gnomAD v3:
1-2408817-C-T
gnomAD v4:
1-2408817-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2408817C>T , CM000663.2:g.2408817C>T | GRCh38 |
| NC_000001.10:g.2340256C>T , CM000663.1:g.2340256C>T | GRCh37 |
| NC_000001.9:g.2330116C>T | NCBI36 |
| NG_008342.1:g.8755G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000288774.8:c.235G>A | ENSP00000288774.3:p.Val79Met | |
| ENST00000447513.7:c.235G>A MANE Select | ENSP00000407922.2:p.Val79Met | |
| ENST00000650293.1:c.189G>A | ||
| ENST00000288774.7:c.235G>A | ENSP00000288774.3:p.Val79Met | |
| ENST00000447513.6:c.235G>A | ENSP00000407922.2:p.Val79Met | |
| ENST00000502666.1:c.440G>A | ENSP00000461951.1:n.440G>A | |
| ENST00000507596.5:c.235G>A | ENSP00000424291.1:p.Val79Met | |
| ENST00000508384.5:c.-198G>A | ENSP00000464289.1:n.-198G>A | |
| ENST00000510434.1:c.235G>A | ENSP00000423051.1:p.Val79Met | |
| ENST00000514502.1:c.*252G>A | ENSP00000425924.1:n.*252G>A | |
| ENST00000515760.1:n.369G>A | ||
| NM_002617.3:c.235G>A | NP_002608.1:p.Val79Met | |
| NM_153818.1:c.235G>A | NP_722540.1:p.Val79Met | |
| XM_011541573.1:c.235G>A | XP_011539875.1:p.Val79Met | |
| XM_011541574.1:c.-198G>A | XP_011539876.1:n.-198G>A | |
| XM_011541575.1:c.-198G>A | XP_011539877.1:n.-198G>A | |
| XM_011541576.1:c.235G>A | XP_011539878.1:p.Val79Met | |
| XR_946666.1:n.355G>A | ||
| XM_011541576.2:c.235G>A | XP_011539878.1:p.Val79Met | |
| XR_946666.2:n.304G>A | ||
| NM_001374425.1:c.235G>A | NP_001361354.1:p.Val79Met | |
| NM_001374426.1:c.-198G>A | NP_001361355.1:n.-198G>A | |
| NM_001374427.1:c.-198G>A | NP_001361356.1:n.-198G>A | |
| NM_002617.4:c.235G>A MANE Select | NP_002608.1:p.Val79Met | |
| NM_153818.2:c.235G>A | NP_722540.1:p.Val79Met | |
| NR_164636.1:n.354G>A |