Linked Data
ClinVar Variation Id:
241026
dbSNP Id:
rs142317242
ExAC:
16:53652991 C / T
gnomAD v2:
16-53652991-C-T
gnomAD v3:
16-53619079-C-T
gnomAD v4:
16-53619079-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.53619079C>T , CM000678.2:g.53619079C>T | GRCh38 |
| NC_000016.9:g.53652991C>T , CM000678.1:g.53652991C>T | GRCh37 |
| NC_000016.8:g.52210492C>T | NCBI36 |
| NG_008991.2:g.89781G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262135.9:c.3322G>A | ENSP00000262135.4:p.Val1108Met | |
| ENST00000565343.2:n.3986G>A | ||
| ENST00000621565.5:c.3424G>A | ENSP00000480698.1:p.Val1142Met | |
| ENST00000647211.2:c.3562G>A MANE Select | ENSP00000493946.1:p.Val1188Met | |
| ENST00000680193.1:c.*322G>A | ENSP00000506379.1:n.*322G>A | |
| ENST00000681587.1:n.1334G>A | ||
| ENST00000262135.8:c.3322G>A | ENSP00000262135.4:p.Val1108Met | |
| ENST00000379925.7:c.3562G>A | ENSP00000369257.3:p.Val1188Met | |
| ENST00000563746.5:c.3460G>A | ENSP00000457889.1:p.Val1154Met | |
| ENST00000564374.5:c.3424G>A | ENSP00000456534.1:p.Val1142Met | |
| ENST00000621565.4:c.3424G>A | ENSP00000480698.1:p.Val1142Met | |
| NM_001127897.1:c.3322G>A | NP_001121369.1:p.Val1108Met | |
| NM_001127897.2:c.3322G>A | NP_001121369.1:p.Val1108Met | |
| NM_001308334.1:c.3424G>A | NP_001295263.1:p.Val1142Met | |
| NM_015272.2:c.3562G>A | NP_056087.2:p.Val1188Met | |
| NM_015272.3:c.3562G>A | NP_056087.2:p.Val1188Met | |
| XM_005255867.1:c.3460G>A | XP_005255924.1:p.Val1154Met | |
| XM_005255868.1:c.3436G>A | XP_005255925.1:p.Val1146Met | |
| XM_005255871.2:c.1669G>A | XP_005255928.1:p.Val557Met | |
| XM_011522968.1:c.3562G>A | XP_011521270.1:p.Val1188Met | |
| XM_011522969.1:c.3436G>A | XP_011521271.1:p.Val1146Met | |
| XM_011522974.1:c.1669G>A | XP_011521276.1:p.Val557Met | |
| XR_933260.1:n.3468G>A | ||
| NM_001127897.3:c.3322G>A | NP_001121369.1:p.Val1108Met | |
| NM_001308334.2:c.3424G>A | NP_001295263.1:p.Val1142Met | |
| NM_001330538.1:c.3460G>A | NP_001317467.1:p.Val1154Met | |
| NM_015272.4:c.3562G>A | NP_056087.2:p.Val1188Met | |
| XM_005255868.2:c.3436G>A | XP_005255925.1:p.Val1146Met | |
| XM_017023094.2:c.3574G>A | XP_016878583.1:p.Val1192Met | |
| XM_017023095.2:c.3334G>A | XP_016878584.1:p.Val1112Met | |
| XM_017023096.2:c.3436G>A | XP_016878585.1:p.Val1146Met | |
| XM_017023098.1:c.1807G>A | XP_016878587.1:p.Val603Met | |
| XM_017023099.1:c.1807G>A | XP_016878588.1:p.Val603Met | |
| XR_933260.3:n.3479G>A | ||
| NM_015272.5:c.3562G>A MANE Select | NP_056087.2:p.Val1188Met | |
| NM_001127897.4:c.3322G>A | NP_001121369.1:p.Val1108Met | |
| NM_001330538.2:c.3460G>A | NP_001317467.1:p.Val1154Met | |
| NM_001308334.3:c.3424G>A | NP_001295263.1:p.Val1142Met |