Linked Data
ClinVar Variation Id:
2672105
ClinVar RCV Id:
RCV003458971
dbSNP Id:
rs1159440697
gnomAD v2:
3-189526315-G-A
gnomAD v3:
3-189808526-G-A
gnomAD v4:
3-189808526-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.189808526G>A , CM000665.2:g.189808526G>A | GRCh38 |
| NC_000003.11:g.189526315G>A , CM000665.1:g.189526315G>A | GRCh37 |
| NC_000003.10:g.191009009G>A | NCBI36 |
| NG_007550.1:g.182100G>A | |
| NG_007550.2:g.182100G>A | |
| NG_007550.3:g.216781G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264731.8:c.579G>A MANE Select | ENSP00000264731.3:p.Thr193= | |
| ENST00000354600.10:c.297G>A MANE Plus Clinical | ENSP00000346614.5:p.Thr99= | |
| ENST00000264731.7:c.579G>A | ENSP00000264731.3:p.Thr193= | |
| ENST00000320472.9:c.579G>A | ENSP00000317510.5:p.Thr193= | |
| ENST00000354600.9:c.297G>A | ENSP00000346614.5:p.Thr99= | |
| ENST00000392460.7:c.579G>A | ENSP00000376253.3:p.Thr193= | |
| ENST00000392461.7:c.297G>A | ENSP00000376254.3:p.Thr99= | |
| ENST00000392463.6:c.297G>A | ENSP00000376256.2:p.Thr99= | |
| ENST00000418709.6:c.579G>A | ENSP00000407144.2:p.Thr193= | |
| ENST00000434928.5:c.297G>A | ENSP00000401661.1:p.Thr99= | |
| ENST00000437221.5:c.297G>A | ENSP00000392488.1:p.Thr99= | |
| ENST00000440651.6:c.579G>A | ENSP00000394337.2:p.Thr193= | |
| ENST00000449992.5:c.42+18684G>A | ENSP00000387839.1:n.42+18684G>A | |
| ENST00000456148.1:c.297G>A | ENSP00000389485.1:p.Thr99= | |
| ENST00000460036.1:n.403G>A | ||
| NM_001114978.1:c.579G>A | NP_001108450.1:p.Thr193= | |
| NM_001114979.1:c.579G>A | NP_001108451.1:p.Thr193= | |
| NM_001114980.1:c.297G>A | NP_001108452.1:p.Thr99= | |
| NM_001114981.1:c.297G>A | NP_001108453.1:p.Thr99= | |
| NM_001114982.1:c.297G>A | NP_001108454.1:p.Thr99= | |
| NM_003722.4:c.579G>A | NP_003713.3:p.Thr193= | |
| XM_005247843.2:c.579G>A | XP_005247900.1:p.Thr193= | |
| XM_005247844.3:c.528G>A | XP_005247901.1:p.Thr176= | |
| XM_005247846.2:c.579G>A | XP_005247903.1:p.Thr193= | |
| XM_011513251.1:c.576G>A | XP_011511553.1:p.Thr192= | |
| XM_011513252.1:c.573G>A | XP_011511554.1:p.Thr191= | |
| XM_011513253.1:c.540G>A | XP_011511555.1:p.Thr180= | |
| NM_001329144.1:c.579G>A | NP_001316073.1:p.Thr193= | |
| NM_001329145.1:c.297G>A | NP_001316074.1:p.Thr99= | |
| NM_001329146.1:c.42+18684G>A | NP_001316075.1:n.42+18684G>A | |
| NM_001329148.1:c.579G>A | NP_001316077.1:p.Thr193= | |
| NM_001329149.1:c.297G>A | NP_001316078.1:p.Thr99= | |
| NM_001329150.1:c.42+18684G>A | NP_001316079.1:n.42+18684G>A | |
| NM_001329964.1:c.573G>A | NP_001316893.1:p.Thr191= | |
| NM_003722.5:c.579G>A MANE Select | NP_003713.3:p.Thr193= | |
| NM_001114978.2:c.579G>A | NP_001108450.1:p.Thr193= | |
| NM_001114979.2:c.579G>A | NP_001108451.1:p.Thr193= | |
| NM_001114980.2:c.297G>A MANE Plus Clinical | NP_001108452.1:p.Thr99= | |
| NM_001114981.2:c.297G>A | NP_001108453.1:p.Thr99= | |
| NM_001114982.2:c.297G>A | NP_001108454.1:p.Thr99= | |
| NM_001329144.2:c.579G>A | NP_001316073.1:p.Thr193= | |
| NM_001329145.2:c.297G>A | NP_001316074.1:p.Thr99= | |
| NM_001329146.2:c.42+18684G>A | NP_001316075.1:n.42+18684G>A | |
| NM_001329148.2:c.579G>A | NP_001316077.1:p.Thr193= | |
| NM_001329149.2:c.297G>A | NP_001316078.1:p.Thr99= | |
| NM_001329150.2:c.42+18684G>A | NP_001316079.1:n.42+18684G>A | |
| NM_001329964.2:c.573G>A | NP_001316893.1:p.Thr191= |