Linked Data
ClinVar Variation Id:
3003045
ClinVar RCV Id:
RCV003860636
dbSNP Id:
rs2141630249
gnomAD v4:
16-9938108-G-A
MyVariant Identifiers:
chr16:g.10031965G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.9938108G>A , CM000678.2:g.9938108G>A | GRCh38 |
| NC_000016.9:g.10031965G>A , CM000678.1:g.10031965G>A | GRCh37 |
| NC_000016.8:g.9939466G>A | NCBI36 |
| NG_011812.1:g.249647C>T | |
| NG_011812.2:g.249647C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330684.4:c.858C>T MANE Select | ENSP00000332549.3:p.Tyr286= | |
| ENST00000535259.6:c.387C>T | ENSP00000441572.3:p.Tyr129= | |
| ENST00000636273.2:n.451C>T | ||
| ENST00000637393.1:c.450C>T | ENSP00000490232.1:p.Tyr150= | |
| ENST00000674742.1:c.387C>T | ENSP00000502200.1:p.Tyr129= | |
| ENST00000675189.1:n.1342C>T | ||
| ENST00000675398.1:c.858C>T | ENSP00000502752.1:p.Tyr286= | |
| ENST00000330684.3:c.858C>T | ENSP00000332549.3:p.Tyr286= | |
| ENST00000396573.6:c.858C>T | ENSP00000379818.2:p.Tyr286= | |
| ENST00000396575.6:c.447C>T | ENSP00000379820.3:p.Tyr149= | |
| ENST00000461292.3:n.497C>T | ||
| ENST00000535259.5:c.447C>T | ENSP00000441572.2:p.Tyr149= | |
| ENST00000562109.5:c.858C>T | ENSP00000454998.1:p.Tyr286= | |
| ENST00000566683.1:n.241-47008C>T | ||
| ENST00000568247.3:n.750C>T | ||
| NM_000833.4:c.858C>T | NP_000824.1:p.Tyr286= | |
| NM_001134407.2:c.858C>T | NP_001127879.1:p.Tyr286= | |
| NM_001134408.2:c.858C>T | NP_001127880.1:p.Tyr286= | |
| XM_011522456.1:c.699C>T | XP_011520758.1:p.Tyr233= | |
| XM_011522457.1:c.600C>T | XP_011520759.1:p.Tyr200= | |
| XM_011522458.1:c.387C>T | XP_011520760.1:p.Tyr129= | |
| XM_011522459.1:c.387C>T | XP_011520761.1:p.Tyr129= | |
| XM_011522460.1:c.387C>T | XP_011520762.1:p.Tyr129= | |
| XM_011522461.1:c.858C>T | XP_011520763.1:p.Tyr286= | |
| XM_011522458.3:c.387C>T | XP_011520760.1:p.Tyr129= | |
| XM_011522461.3:c.858C>T | XP_011520763.1:p.Tyr286= | |
| XM_017023172.1:c.1014C>T | XP_016878661.1:p.Tyr338= | |
| XM_017023173.1:c.1014C>T | XP_016878662.1:p.Tyr338= | |
| NM_001134407.3:c.858C>T MANE Select | NP_001127879.1:p.Tyr286= | |
| NM_000833.5:c.858C>T | NP_000824.1:p.Tyr286= |