Linked Data
ClinVar Variation Id:
216750
dbSNP Id:
rs863224783
gnomAD v2:
16-23632693-T-C
gnomAD v3:
16-23621372-T-C
gnomAD v4:
16-23621372-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23621372T>C , CM000678.2:g.23621372T>C | GRCh38 |
| NC_000016.9:g.23632693T>C , CM000678.1:g.23632693T>C | GRCh37 |
| NC_000016.8:g.23540194T>C | NCBI36 |
| NG_007406.1:g.24986A>G , LRG_308:g.24986A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.3109A>G | ENSP00000460666.3:p.Ile1037Val | |
| ENST00000565038.2:c.*584A>G | ENSP00000459882.2:n.*584A>G | |
| ENST00000566069.6:c.3103A>G | ENSP00000459237.2:p.Ile1035Val | |
| ENST00000697377.2:c.2947A>G | ENSP00000513286.2:p.Ile983Val | |
| ENST00000697379.2:c.3109A>G | ENSP00000513287.2:p.Ile1037Val | |
| ENST00000561514.2:c.2218A>G | ENSP00000460666.2:p.Ile740Val | |
| ENST00000697374.1:c.2218A>G | ENSP00000513284.1:p.Ile740Val | |
| ENST00000697375.1:n.4450A>G | ||
| ENST00000697376.1:c.2218A>G | ENSP00000513285.1:p.Ile740Val | |
| ENST00000697377.1:c.2056A>G | ENSP00000513286.1:p.Ile686Val | |
| ENST00000697378.1:n.3623A>G | ||
| ENST00000697379.1:c.2218A>G | ENSP00000513287.1:p.Ile740Val | |
| ENST00000697380.1:n.2395A>G | ||
| ENST00000697381.1:n.1798A>G | ||
| ENST00000697382.1:c.2218A>G | ENSP00000513288.1:p.Ile740Val | |
| ENST00000697383.1:c.637A>G | ENSP00000513289.1:p.Ile213Val | |
| ENST00000261584.9:c.3103A>G MANE Select | ENSP00000261584.4:p.Ile1035Val | |
| ENST00000261584.8:c.3103A>G | ENSP00000261584.4:p.Ile1035Val | |
| ENST00000566069.5:c.18A>G | ||
| ENST00000568219.5:c.2218A>G | ENSP00000454703.2:p.Ile740Val | |
| NM_024675.3:c.3103A>G , LRG_308t1:c.3103A>G | NP_078951.2:p.Ile1035Val | |
| XM_011545946.1:c.3109A>G | XP_011544248.1:p.Ile1037Val | |
| XM_011545947.1:c.3109A>G | XP_011544249.1:p.Ile1037Val | |
| XM_011545948.1:c.2218A>G | XP_011544250.1:p.Ile740Val | |
| XR_950851.1:n.3899A>G | ||
| XM_011545946.2:c.3109A>G | XP_011544248.1:p.Ile1037Val | |
| XM_011545947.2:c.3109A>G | XP_011544249.1:p.Ile1037Val | |
| XM_011545948.2:c.2218A>G | XP_011544250.1:p.Ile740Val | |
| XM_017023671.1:c.3109A>G | XP_016879160.1:p.Ile1037Val | |
| XM_017023672.2:c.3103A>G | XP_016879161.1:p.Ile1035Val | |
| XM_017023673.2:c.3103A>G | XP_016879162.1:p.Ile1035Val | |
| NM_024675.4:c.3103A>G MANE Select | NP_078951.2:p.Ile1035Val |