Linked Data
dbSNP Id:
rs1279885534
gnomAD v2:
12-8814677-C-G
gnomAD v4:
12-8662081-C-G
COSMIC:
COSM6138346
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.8662081C>G , CM000674.2:g.8662081C>G | GRCh38 |
| NC_000012.11:g.8814677C>G , CM000674.1:g.8814677C>G | GRCh37 |
| NC_000012.10:g.8705944C>G | NCBI36 |
| NG_041814.1:g.5808G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359478.7:c.24G>C MANE Select | ENSP00000352455.2:p.Val8= | |
| ENST00000359478.6:c.24G>C | ENSP00000352455.2:p.Val8= | |
| ENST00000396549.6:c.24G>C | ENSP00000379798.2:p.Val8= | |
| ENST00000433590.6:c.24G>C | ENSP00000411997.2:p.Val8= | |
| ENST00000534833.5:n.75G>C | ||
| ENST00000535336.5:c.24G>C | ENSP00000438525.1:p.Val8= | |
| ENST00000537009.5:c.24G>C | ENSP00000439289.1:p.Val8= | |
| ENST00000537128.1:n.288G>C | ||
| ENST00000538107.5:n.288G>C | ||
| ENST00000540087.5:c.24G>C | ENSP00000440496.1:p.Val8= | |
| ENST00000543369.5:c.24G>C | ENSP00000441492.1:p.Val8= | |
| ENST00000544211.5:c.24G>C | ENSP00000443839.1:p.Val8= | |
| ENST00000544889.1:c.24G>C | ENSP00000445799.1:p.Val8= | |
| NM_001297709.1:c.24G>C | NP_001284638.1:p.Val8= | |
| NM_001297710.1:c.24G>C | NP_001284639.1:p.Val8= | |
| NM_001297711.1:c.24G>C | NP_001284640.1:p.Val8= | |
| NM_001297712.1:c.24G>C | NP_001284641.1:p.Val8= | |
| NM_003480.3:c.24G>C | NP_003471.1:p.Val8= | |
| NR_123733.1:n.288G>C | ||
| NR_123734.1:n.288G>C | ||
| NM_003480.4:c.24G>C MANE Select | NP_003471.1:p.Val8= | |
| NM_001297709.2:c.24G>C | NP_001284638.1:p.Val8= | |
| NM_001297710.2:c.24G>C | NP_001284639.1:p.Val8= | |
| NM_001297711.2:c.24G>C | NP_001284640.1:p.Val8= | |
| NM_001297712.2:c.24G>C | NP_001284641.1:p.Val8= | |
| NR_123733.2:n.226G>C | ||
| NR_123734.2:n.226G>C |