Linked Data
ClinVar Variation Id:
589263
dbSNP Id:
rs901717931
gnomAD v2:
16-10031919-C-T
gnomAD v3:
16-9938062-C-T
gnomAD v4:
16-9938062-C-T
COSMIC:
COSM180469
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.9938062C>T , CM000678.2:g.9938062C>T | GRCh38 |
| NC_000016.9:g.10031919C>T , CM000678.1:g.10031919C>T | GRCh37 |
| NC_000016.8:g.9939420C>T | NCBI36 |
| NG_011812.1:g.249693G>A | |
| NG_011812.2:g.249693G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330684.4:c.904G>A MANE Select | ENSP00000332549.3:p.Ala302Thr | |
| ENST00000535259.6:c.433G>A | ENSP00000441572.3:p.Ala145Thr | |
| ENST00000636273.2:n.497G>A | ||
| ENST00000637393.1:c.496G>A | ENSP00000490232.1:p.Ala166Thr | |
| ENST00000674742.1:c.433G>A | ENSP00000502200.1:p.Ala145Thr | |
| ENST00000675189.1:n.1388G>A | ||
| ENST00000675398.1:c.904G>A | ENSP00000502752.1:p.Ala302Thr | |
| ENST00000330684.3:c.904G>A | ENSP00000332549.3:p.Ala302Thr | |
| ENST00000396573.6:c.904G>A | ENSP00000379818.2:p.Ala302Thr | |
| ENST00000396575.6:c.493G>A | ENSP00000379820.3:p.Ala165Thr | |
| ENST00000461292.3:n.543G>A | ||
| ENST00000535259.5:c.493G>A | ENSP00000441572.2:p.Ala165Thr | |
| ENST00000562109.5:c.904G>A | ENSP00000454998.1:p.Ala302Thr | |
| ENST00000566683.1:n.241-46962G>A | ||
| ENST00000568247.3:n.796G>A | ||
| NM_000833.4:c.904G>A | NP_000824.1:p.Ala302Thr | |
| NM_001134407.2:c.904G>A | NP_001127879.1:p.Ala302Thr | |
| NM_001134408.2:c.904G>A | NP_001127880.1:p.Ala302Thr | |
| XM_011522456.1:c.745G>A | XP_011520758.1:p.Ala249Thr | |
| XM_011522457.1:c.646G>A | XP_011520759.1:p.Ala216Thr | |
| XM_011522458.1:c.433G>A | XP_011520760.1:p.Ala145Thr | |
| XM_011522459.1:c.433G>A | XP_011520761.1:p.Ala145Thr | |
| XM_011522460.1:c.433G>A | XP_011520762.1:p.Ala145Thr | |
| XM_011522461.1:c.904G>A | XP_011520763.1:p.Ala302Thr | |
| XM_011522458.3:c.433G>A | XP_011520760.1:p.Ala145Thr | |
| XM_011522461.3:c.904G>A | XP_011520763.1:p.Ala302Thr | |
| XM_017023172.1:c.1060G>A | XP_016878661.1:p.Ala354Thr | |
| XM_017023173.1:c.1060G>A | XP_016878662.1:p.Ala354Thr | |
| NM_001134407.3:c.904G>A MANE Select | NP_001127879.1:p.Ala302Thr | |
| NM_000833.5:c.904G>A | NP_000824.1:p.Ala302Thr |