Linked Data
ClinVar Variation Id:
2042919
dbSNP Id:
rs376389208
ExAC:
17:41063339 G / A
gnomAD v2:
17-41063339-G-A
gnomAD v3:
17-42911322-G-A
gnomAD v4:
17-42911322-G-A
COSMIC:
COSM2155607
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911322G>A , CM000679.2:g.42911322G>A | GRCh38 |
| NC_000017.10:g.41063339G>A , CM000679.1:g.41063339G>A | GRCh37 |
| NC_000017.9:g.38316865G>A | NCBI36 |
| NG_011808.1:g.15525G>A , LRG_147:g.15525G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.970G>A MANE Select | ENSP00000253801.1:p.Val324Ile | |
| ENST00000253801.6:c.970G>A | ENSP00000253801.1:p.Val324Ile | |
| ENST00000585489.1:c.*362G>A | ENSP00000466202.1:n.*362G>A | |
| ENST00000592383.5:c.*362G>A | ENSP00000465958.1:n.*362G>A | |
| NM_000151.3:c.970G>A | NP_000142.2:p.Val324Ile | |
| NM_001270397.1:c.*362G>A | NP_001257326.1:n.*362G>A | |
| NM_000151.4:c.970G>A MANE Select | NP_000142.2:p.Val324Ile | |
| NM_001270397.2:c.*362G>A | NP_001257326.1:n.*362G>A |