Linked Data
ClinVar Variation Id:
1368548
ClinVar RCV Id:
RCV002551032
dbSNP Id:
rs1200152449
gnomAD v2:
16-50746200-T-C
gnomAD v3:
16-50712289-T-C
gnomAD v4:
16-50712289-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.50712289T>C , CM000678.2:g.50712289T>C | GRCh38 |
| NC_000016.9:g.50746200T>C , CM000678.1:g.50746200T>C | GRCh37 |
| NC_000016.8:g.49303701T>C | NCBI36 |
| NG_007508.1:g.20151T>C , LRG_177:g.20151T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000641284.2:c.2297T>C | ENSP00000493088.1:p.Val766Ala | |
| ENST00000646677.2:c.2297T>C | ENSP00000496533.1:p.Val766Ala | |
| ENST00000697425.1:c.96T>C | ||
| ENST00000697426.1:c.96T>C | ||
| ENST00000697427.1:c.96T>C | ||
| ENST00000641284.1:c.2297T>C | ENSP00000493088.1:p.Val766Ala | |
| ENST00000646677.1:c.2297T>C | ENSP00000496533.1:p.Val766Ala | |
| ENST00000647318.2:c.2297T>C MANE Select | ENSP00000495993.1:p.Val766Ala | |
| ENST00000300589.6:c.2378T>C | ENSP00000300589.2:p.Val793Ala | |
| ENST00000524712.5:c.96T>C | ||
| ENST00000527052.5:c.96T>C | ||
| ENST00000529633.5:c.96T>C | ||
| ENST00000534057.1:c.96T>C | ||
| ENST00000534067.5:c.96T>C | ||
| NM_001293557.1:c.2297T>C | NP_001280486.1:p.Val766Ala | |
| NM_022162.2:c.2378T>C | NP_071445.1:p.Val793Ala | |
| XM_005256084.2:c.2297T>C | XP_005256141.1:p.Val766Ala | |
| XM_006721242.2:c.2297T>C | XP_006721305.1:p.Val766Ala | |
| XM_006721243.2:c.2297T>C | XP_006721306.1:p.Val766Ala | |
| XM_011523257.1:c.1874T>C | XP_011521559.1:p.Val625Ala | |
| XM_011523258.1:c.1874T>C | XP_011521560.1:p.Val625Ala | |
| XM_011523259.1:c.1712T>C | XP_011521561.1:p.Val571Ala | |
| XM_011523260.1:c.2297T>C | XP_011521562.1:p.Val766Ala | |
| XM_011523261.1:c.2297T>C | XP_011521563.1:p.Val766Ala | |
| XR_429725.2:n.2387T>C | ||
| XR_429726.2:n.2387T>C | ||
| XR_933387.1:n.2387T>C | ||
| XM_005256084.4:c.2297T>C | XP_005256141.1:p.Val766Ala | |
| XM_006721242.4:c.2297T>C | XP_006721305.1:p.Val766Ala | |
| XM_006721243.4:c.2297T>C | XP_006721306.1:p.Val766Ala | |
| XM_011523259.2:c.1712T>C | XP_011521561.1:p.Val571Ala | |
| XM_011523260.3:c.2297T>C | XP_011521562.1:p.Val766Ala | |
| XM_011523261.2:c.2297T>C | XP_011521563.1:p.Val766Ala | |
| XM_017023535.1:c.1805T>C | XP_016879024.1:p.Val602Ala | |
| XM_017023536.1:c.1712T>C | XP_016879025.1:p.Val571Ala | |
| XM_017023537.1:c.1712T>C | XP_016879026.1:p.Val571Ala | |
| XM_017023538.1:c.1712T>C | XP_016879027.1:p.Val571Ala | |
| XR_429725.3:n.2340T>C | ||
| XR_429726.3:n.2340T>C | ||
| XR_933387.2:n.2340T>C | ||
| NM_001293557.2:c.2297T>C | NP_001280486.1:p.Val766Ala | |
| NM_001370466.1:c.2297T>C MANE Select | NP_001357395.1:p.Val766Ala | |
| NM_022162.3:c.2378T>C | NP_071445.1:p.Val793Ala | |
| NR_163434.1:n.2362T>C |