Linked Data
ClinVar Variation Id:
767235
dbSNP Id:
rs766088261
ExAC:
3:10191538 A / G
gnomAD v2:
3-10191538-A-G
gnomAD v3:
3-10149854-A-G
gnomAD v4:
3-10149854-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10149854A>G , CM000665.2:g.10149854A>G | GRCh38 |
| NC_000003.11:g.10191538A>G , CM000665.1:g.10191538A>G | GRCh37 |
| NC_000003.10:g.10166538A>G | NCBI36 |
| NG_008212.3:g.13220A>G , LRG_322:g.13220A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*208A>G | ENSP00000512434.1:n.*208A>G | |
| ENST00000696143.1:c.667A>G | ENSP00000512435.1:n.667A>G | |
| ENST00000696153.1:c.642A>G | ENSP00000512444.1:p.Arg214= | |
| ENST00000256474.3:c.531A>G MANE Select | ENSP00000256474.3:p.Arg177= | |
| ENST00000256474.2:c.531A>G | ENSP00000256474.2:p.Arg177= | |
| ENST00000345392.2:c.408A>G | ENSP00000344757.2:p.Arg136= | |
| ENST00000477538.1:n.667A>G | ||
| NM_000551.3:c.531A>G , LRG_322t1:c.531A>G | NP_000542.1:p.Arg177= | |
| NM_198156.2:c.408A>G | NP_937799.1:p.Arg136= | |
| NM_001354723.1:c.*85A>G | NP_001341652.1:n.*85A>G | |
| NM_000551.4:c.531A>G MANE Select | NP_000542.1:p.Arg177= | |
| NM_001354723.2:c.*85A>G | NP_001341652.1:n.*85A>G | |
| NM_198156.3:c.408A>G | NP_937799.1:p.Arg136= |