Linked Data
ClinVar Variation Id:
446825
dbSNP Id:
rs74033734
ExAC:
16:89351654 C / G
gnomAD v2:
16-89351654-C-G
gnomAD v3:
16-89285246-C-G
gnomAD v4:
16-89285246-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89285246C>G , CM000678.2:g.89285246C>G | GRCh38 |
| NC_000016.9:g.89351654C>G , CM000678.1:g.89351654C>G | GRCh37 |
| NC_000016.8:g.87879155C>G | NCBI36 |
| NG_032003.1:g.210316G>C | |
| NG_032003.2:g.210316G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000301030.10:c.1296G>C MANE Select | ENSP00000301030.4:p.Thr432= | |
| ENST00000330736.10:c.*1099G>C | ENSP00000330815.5:n.*1099G>C | |
| ENST00000378330.7:c.1296G>C | ENSP00000367581.2:p.Thr432= | |
| ENST00000568100.2:n.1002G>C | ||
| ENST00000642443.1:c.921G>C | ENSP00000493644.1:p.Thr307= | |
| ENST00000642600.1:c.1296G>C | ENSP00000495226.1:p.Thr432= | |
| ENST00000644285.1:c.744+3282G>C | ENSP00000496476.1:n.744+3282G>C | |
| ENST00000645212.1:n.3068G>C | ||
| ENST00000646345.1:n.1288G>C | ||
| ENST00000301030.8:c.1296G>C | ENSP00000301030.4:p.Thr432= | |
| ENST00000330736.9:c.*1099G>C | ENSP00000330815.5:n.*1099G>C | |
| ENST00000378330.6:c.1296G>C | ENSP00000367581.2:p.Thr432= | |
| ENST00000562194.1:c.151+3282G>C | ||
| ENST00000568100.1:n.847G>C | ||
| ENST00000613312.4:c.*194G>C | ENSP00000478018.1:n.*194G>C | |
| NM_001256182.1:c.1296G>C | NP_001243111.1:p.Thr432= | |
| NM_001256183.1:c.1296G>C | NP_001243112.1:p.Thr432= | |
| NM_013275.5:c.1296G>C | NP_037407.4:p.Thr432= | |
| XM_006721181.1:c.1194G>C | XP_006721244.1:p.Thr398= | |
| XM_006721184.2:c.999G>C | XP_006721247.1:p.Thr333= | |
| XM_011523051.1:c.1296G>C | XP_011521353.1:p.Thr432= | |
| XM_011523052.1:c.1296G>C | XP_011521354.1:p.Thr432= | |
| XM_011523053.1:c.1296G>C | XP_011521355.1:p.Thr432= | |
| XM_011523054.1:c.1194G>C | XP_011521356.1:p.Thr398= | |
| XM_011523055.1:c.1194G>C | XP_011521357.1:p.Thr398= | |
| XM_011523056.1:c.1167G>C | XP_011521358.1:p.Thr389= | |
| XM_011523057.1:c.1296G>C | XP_011521359.1:p.Thr432= | |
| XM_011523051.3:c.1296G>C | XP_011521353.1:p.Thr432= | |
| XM_011523053.2:c.1296G>C | XP_011521355.1:p.Thr432= | |
| XM_011523054.2:c.1194G>C | XP_011521356.1:p.Thr398= | |
| XM_011523055.2:c.1194G>C | XP_011521357.1:p.Thr398= | |
| XM_011523056.2:c.1167G>C | XP_011521358.1:p.Thr389= | |
| XM_011523057.2:c.1296G>C | XP_011521359.1:p.Thr432= | |
| XM_017023182.2:c.1296G>C | XP_016878671.1:p.Thr432= | |
| XM_017023183.1:c.1296G>C | XP_016878672.1:p.Thr432= | |
| XM_017023184.1:c.1296G>C | XP_016878673.1:p.Thr432= | |
| XM_017023185.1:c.1296G>C | XP_016878674.1:p.Thr432= | |
| XM_017023186.1:c.1296G>C | XP_016878675.1:p.Thr432= | |
| XM_017023187.1:c.1296G>C | XP_016878676.1:p.Thr432= | |
| XM_024450244.1:c.1194G>C | XP_024306012.1:p.Thr398= | |
| NM_013275.6:c.1296G>C MANE Select | NP_037407.4:p.Thr432= | |
| NM_001256182.2:c.1296G>C | NP_001243111.1:p.Thr432= | |
| NM_001256183.2:c.1296G>C | NP_001243112.1:p.Thr432= |