Linked Data
ClinVar Variation Id:
1385746
dbSNP Id:
rs564022938
ExAC:
8:99170233 G / A
gnomAD v2:
8-99170233-G-A
gnomAD v3:
8-98158005-G-A
gnomAD v4:
8-98158005-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.98158005G>A , CM000670.2:g.98158005G>A | GRCh38 |
| NC_000008.10:g.99170233G>A , CM000670.1:g.99170233G>A | GRCh37 |
| NC_000008.9:g.99239409G>A | NCBI36 |
| NG_052869.1:g.45713G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401707.7:c.2809G>A MANE Select | ENSP00000385787.2:p.Val937Met | |
| ENST00000349693.3:c.2809G>A | ENSP00000339529.3:p.Val937Met | |
| ENST00000401707.6:c.2809G>A | ENSP00000385787.2:p.Val937Met | |
| NM_001145860.1:c.2809G>A | NP_001139332.1:p.Val937Met | |
| NM_001145861.1:c.2809G>A | NP_001139333.1:p.Val937Met | |
| NM_015029.2:c.2809G>A | NP_055844.2:p.Val937Met | |
| NM_001145860.2:c.2809G>A MANE Select | NP_001139332.1:p.Val937Met | |
| NM_001145861.2:c.2809G>A | NP_001139333.1:p.Val937Met | |
| NM_015029.3:c.2809G>A | NP_055844.2:p.Val937Met |