Linked Data
ClinVar Variation Id:
312820
dbSNP Id:
rs539843065
ExAC:
14:23245109 T / C
gnomAD v2:
14-23245109-T-C
gnomAD v3:
14-22775900-T-C
gnomAD v4:
14-22775900-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.22775900T>C , CM000676.2:g.22775900T>C | GRCh38 |
| NC_000014.8:g.23245109T>C , CM000676.1:g.23245109T>C | GRCh37 |
| NC_000014.7:g.22314949T>C | NCBI36 |
| NG_012851.2:g.58921A>G , LRG_695:g.58921A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555911.2:c.931A>G | ENSP00000452551.2:p.Ile311Val | |
| ENST00000698939.1:c.807A>G | ENSP00000514047.1:p.Gly269= | |
| ENST00000397532.9:c.931A>G | ENSP00000380666.4:p.Ile311Val | |
| ENST00000674313.1:c.931A>G MANE Select | ENSP00000501493.1:p.Ile311Val | |
| ENST00000285850.11:c.931A>G | ENSP00000285850.7:p.Ile311Val | |
| ENST00000397528.8:c.931A>G | ENSP00000380662.4:p.Ile311Val | |
| ENST00000397529.6:c.931A>G | ENSP00000380663.2:p.Ile311Val | |
| ENST00000397532.7:c.931A>G | ENSP00000380666.3:p.Ile311Val | |
| ENST00000554061.5:n.602A>G | ||
| ENST00000554517.5:c.133A>G | ENSP00000452083.1:p.Ile45Val | |
| ENST00000555702.5:c.931A>G | ENSP00000451881.1:p.Ile311Val | |
| ENST00000556287.5:c.894+295A>G | ENSP00000450715.1:n.894+295A>G | |
| ENST00000556350.1:c.75A>G | ||
| NM_001126105.2:c.931A>G , LRG_695t1:c.931A>G | NP_001119577.1:p.Ile311Val | |
| NM_001126106.2:c.931A>G , LRG_695t2:c.931A>G | NP_001119578.1:p.Ile311Val | |
| NR_040448.1:n.1546A>G | ||
| XM_006720302.1:c.931A>G | XP_006720365.1:p.Ile311Val | |
| XM_011537298.1:c.931A>G | XP_011535600.1:p.Ile311Val | |
| XM_011537299.1:c.931A>G | XP_011535601.1:p.Ile311Val | |
| XM_006720302.2:c.931A>G | XP_006720365.1:p.Ile311Val | |
| XM_011537298.3:c.931A>G | XP_011535600.1:p.Ile311Val | |
| NM_001126105.3:c.931A>G | NP_001119577.1:p.Ile311Val | |
| NM_001126106.4:c.931A>G | NP_001119578.1:p.Ile311Val | |
| NM_003982.4:c.931A>G MANE Select | NP_003973.3:p.Ile311Val |