Linked Data
ClinVar Variation Id:
210963
dbSNP Id:
rs62640002
ExAC:
9:37784849 C / T
gnomAD v2:
9-37784849-C-T
gnomAD v3:
9-37784852-C-T
gnomAD v4:
9-37784852-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.37784852C>T , CM000671.2:g.37784852C>T | GRCh38 |
| NC_000009.11:g.37784849C>T , CM000671.1:g.37784849C>T | GRCh37 |
| NC_000009.10:g.37774849C>T | NCBI36 |
| NG_032780.1:g.5241G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327304.10:c.193G>A MANE Select | ENSP00000323046.4:p.Val65Ile | |
| ENST00000678095.1:c.-70-789G>A | ENSP00000503205.1:n.-70-789G>A | |
| ENST00000678588.1:n.213G>A | ||
| ENST00000679059.1:c.193G>A | ENSP00000503947.1:p.Val65Ile | |
| ENST00000327304.9:c.193G>A | ENSP00000323046.4:p.Val65Ile | |
| ENST00000396521.3:c.193G>A | ENSP00000379775.3:p.Val65Ile | |
| ENST00000465229.5:c.193G>A | ENSP00000418422.1:p.Val65Ile | |
| ENST00000482614.5:n.86-789G>A | ||
| ENST00000489414.5:n.44-789G>A | ||
| ENST00000540557.1:c.*761-789G>A | ENSP00000457548.1:n.*761-789G>A | |
| NM_001002269.2:c.193G>A | NP_001002269.1:p.Val65Ile | |
| NM_016042.3:c.193G>A | NP_057126.2:p.Val65Ile | |
| NM_016042.4:c.193G>A MANE Select | NP_057126.2:p.Val65Ile |