Linked Data
ClinVar Variation Id:
219282
dbSNP Id:
rs145757313
ExAC:
9:137591886 G / A
gnomAD v2:
9-137591886-G-A
gnomAD v3:
9-134700040-G-A
gnomAD v4:
9-134700040-G-A
COSMIC:
COSM243802
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134700040G>A , CM000671.2:g.134700040G>A | GRCh38 |
| NC_000009.11:g.137591886G>A , CM000671.1:g.137591886G>A | GRCh37 |
| NC_000009.10:g.136731707G>A | NCBI36 |
| NG_008030.1:g.63235G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.409G>A | ENSP00000360885.4:p.Val137Ile | |
| ENST00000371817.8:c.409G>A MANE Select | ENSP00000360882.3:p.Val137Ile | |
| ENST00000371817.7:c.409G>A | ENSP00000360882.3:p.Val137Ile | |
| ENST00000464187.1:n.831G>A | ||
| ENST00000618395.4:c.409G>A | ENSP00000481360.1:p.Val137Ile | |
| NM_000093.4:c.409G>A | NP_000084.3:p.Val137Ile | |
| NM_001278074.1:c.409G>A | NP_001265003.1:p.Val137Ile | |
| XR_929712.1:n.811G>A | ||
| XR_929713.1:n.811G>A | ||
| XM_017014266.2:c.409G>A | XP_016869755.1:p.Val137Ile | |
| XR_001746183.1:n.807G>A | ||
| NM_000093.5:c.409G>A MANE Select | NP_000084.3:p.Val137Ile |