Linked Data
ClinVar Variation Id:
284586
dbSNP Id:
rs763348222
ExAC:
2:238257288 C / T
gnomAD v2:
2-238257288-C-T
gnomAD v3:
2-237348645-C-T
gnomAD v4:
2-237348645-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237348645C>T , CM000664.2:g.237348645C>T | GRCh38 |
| NC_000002.11:g.238257288C>T , CM000664.1:g.238257288C>T | GRCh37 |
| NC_000002.10:g.237922027C>T | NCBI36 |
| NG_008676.1:g.70563G>A , LRG_473:g.70563G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000353578.9:c.6280G>A | ENSP00000315873.4:p.Gly2094Arg | |
| ENST00000295550.9:c.6898G>A MANE Select | ENSP00000295550.4:p.Gly2300Arg | |
| ENST00000295550.8:c.6898G>A | ENSP00000295550.4:p.Gly2300Arg | |
| ENST00000347401.7:c.5077G>A | ENSP00000315609.4:p.Gly1693Arg | |
| ENST00000353578.8:c.6280G>A | ENSP00000315873.4:p.Gly2094Arg | |
| ENST00000409809.5:c.6280G>A | ENSP00000386844.1:p.Gly2094Arg | |
| ENST00000472056.5:c.5077G>A | ENSP00000418285.1:p.Gly1693Arg | |
| ENST00000491769.1:n.1152G>A | ||
| NM_004369.3:c.6898G>A , LRG_473t1:c.6898G>A | NP_004360.2:p.Gly2300Arg | |
| NM_057166.4:c.5077G>A | NP_476507.3:p.Gly1693Arg | |
| NM_057167.3:c.6280G>A | NP_476508.2:p.Gly2094Arg | |
| XM_005246065.1:c.6298G>A | XP_005246122.1:p.Gly2100Arg | |
| XM_005246066.1:c.5677G>A | XP_005246123.1:p.Gly1893Arg | |
| XM_006712253.1:c.6397G>A | XP_006712316.1:p.Gly2133Arg | |
| XM_011510574.1:c.6895G>A | XP_011508876.1:p.Gly2299Arg | |
| XM_011510575.1:c.4492G>A | XP_011508877.1:p.Gly1498Arg | |
| XM_017003304.1:c.4492G>A | XP_016858793.1:p.Gly1498Arg | |
| XM_024452684.1:c.5677G>A | XP_024308452.1:p.Gly1893Arg | |
| NM_004369.4:c.6898G>A MANE Select | NP_004360.2:p.Gly2300Arg | |
| NM_057166.5:c.5077G>A | NP_476507.3:p.Gly1693Arg | |
| NM_057167.4:c.6280G>A | NP_476508.2:p.Gly2094Arg |