Linked Data
ClinVar Variation Id:
476560
dbSNP Id:
rs115116398
ExAC:
2:238249358 C / T
gnomAD v2:
2-238249358-C-T
gnomAD v3:
2-237340715-C-T
gnomAD v4:
2-237340715-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237340715C>T , CM000664.2:g.237340715C>T | GRCh38 |
| NC_000002.11:g.238249358C>T , CM000664.1:g.238249358C>T | GRCh37 |
| NC_000002.10:g.237914097C>T | NCBI36 |
| NG_008676.1:g.78493G>A , LRG_473:g.78493G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347401.8:c.846G>A | ||
| ENST00000353578.9:c.7583G>A | ENSP00000315873.4:p.Arg2528Gln | |
| ENST00000682957.1:c.204G>A | ||
| ENST00000684508.1:n.468G>A | ||
| ENST00000295550.9:c.8201G>A MANE Select | ENSP00000295550.4:p.Arg2734Gln | |
| ENST00000295550.8:c.8201G>A | ENSP00000295550.4:p.Arg2734Gln | |
| ENST00000347401.7:c.6377G>A | ENSP00000315609.4:p.Arg2126Gln | |
| ENST00000353578.8:c.7583G>A | ENSP00000315873.4:p.Arg2528Gln | |
| ENST00000409809.5:c.7583G>A | ENSP00000386844.1:p.Arg2528Gln | |
| ENST00000472056.5:c.6380G>A | ENSP00000418285.1:p.Arg2127Gln | |
| ENST00000491769.1:n.4643G>A | ||
| NM_004369.3:c.8201G>A , LRG_473t1:c.8201G>A | NP_004360.2:p.Arg2734Gln | |
| NM_057166.4:c.6380G>A | NP_476507.3:p.Arg2127Gln | |
| NM_057167.3:c.7583G>A | NP_476508.2:p.Arg2528Gln | |
| XM_005246065.1:c.7601G>A | XP_005246122.1:p.Arg2534Gln | |
| XM_005246066.1:c.6980G>A | XP_005246123.1:p.Arg2327Gln | |
| XM_006712253.1:c.7700G>A | XP_006712316.1:p.Arg2567Gln | |
| XM_011510574.1:c.8198G>A | XP_011508876.1:p.Arg2733Gln | |
| XM_011510575.1:c.5795G>A | XP_011508877.1:p.Arg1932Gln | |
| XM_017003304.1:c.5795G>A | XP_016858793.1:p.Arg1932Gln | |
| XM_024452684.1:c.6980G>A | XP_024308452.1:p.Arg2327Gln | |
| NM_004369.4:c.8201G>A MANE Select | NP_004360.2:p.Arg2734Gln | |
| NM_057166.5:c.6380G>A | NP_476507.3:p.Arg2127Gln | |
| NM_057167.4:c.7583G>A | NP_476508.2:p.Arg2528Gln |