Linked Data
ClinVar Variation Id:
161343
dbSNP Id:
rs138925964
ExAC:
3:93598123 C / T
gnomAD v2:
3-93598123-C-T
gnomAD v3:
3-93879279-C-T
gnomAD v4:
3-93879279-C-T
PubMed:
PMID:27652279
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.93879279C>T , CM000665.2:g.93879279C>T | GRCh38 |
| NC_000003.11:g.93598123C>T , CM000665.1:g.93598123C>T | GRCh37 |
| NC_000003.10:g.95080813C>T | NCBI36 |
| NG_009813.1:g.99812G>A , LRG_572:g.99812G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000348974.5:c.1528G>A | ENSP00000330021.7:p.Val510Met | |
| ENST00000394236.9:c.1528G>A MANE Select | ENSP00000377783.3:p.Val510Met | |
| ENST00000407433.6:c.1483G>A | ENSP00000385794.2:p.Val495Met | |
| ENST00000647936.1:c.1528G>A | ENSP00000496822.1:p.Val510Met | |
| ENST00000648381.1:n.1696G>A | ||
| ENST00000648853.1:c.1486G>A | ENSP00000497262.1:p.Val496Met | |
| ENST00000649103.1:c.1627G>A | ENSP00000497962.1:n.1627G>A | |
| ENST00000649585.1:c.471G>A | ENSP00000498163.1:n.471G>A | |
| ENST00000650591.1:c.1624G>A | ENSP00000497376.1:p.Val542Met | |
| ENST00000394236.7:c.1528G>A | ENSP00000377783.3:p.Val510Met | |
| ENST00000407433.5:c.1135G>A | ENSP00000385794.1:p.Val379Met | |
| NM_000313.3:c.1528G>A , LRG_572t1:c.1528G>A | NP_000304.2:p.Val510Met | |
| NM_001314077.1:c.1624G>A , LRG_572t2:c.1624G>A | NP_001301006.1:p.Val542Met | |
| NM_000313.4:c.1528G>A MANE Select | NP_000304.2:p.Val510Met | |
| NM_001314077.2:c.1624G>A | NP_001301006.1:p.Val542Met |