Linked Data
ClinVar Variation Id:
497484
dbSNP Id:
rs372430349
ExAC:
10:123325039 C / T
gnomAD v2:
10-123325039-C-T
gnomAD v3:
10-121565525-C-T
gnomAD v4:
10-121565525-C-T
COSMIC:
COSM49174
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.121565525C>T , CM000672.2:g.121565525C>T | GRCh38 |
| NC_000010.10:g.123325039C>T , CM000672.1:g.123325039C>T | GRCh37 |
| NC_000010.9:g.123315029C>T | NCBI36 |
| NG_012449.1:g.37934G>A | |
| NG_012449.2:g.37934G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000457416.7:c.289G>A MANE Plus Clinical | ENSP00000410294.2:p.Ala97Thr | |
| ENST00000351936.11:c.289G>A | ENSP00000309878.10:p.Ala97Thr | |
| ENST00000682400.1:n.110-14066G>A | ||
| ENST00000682550.1:c.110-14066G>A | ENSP00000507633.1:n.110-14066G>A | |
| ENST00000683035.1:c.289G>A | ENSP00000507074.1:p.Ala97Thr | |
| ENST00000683211.1:c.289G>A | ENSP00000508257.1:p.Ala97Thr | |
| ENST00000683250.1:c.110-14066G>A | ENSP00000506847.1:n.110-14066G>A | |
| ENST00000683678.1:n.289G>A | ||
| ENST00000684153.1:c.110-14066G>A | ENSP00000506937.1:n.110-14066G>A | |
| ENST00000358487.10:c.289G>A MANE Select | ENSP00000351276.6:p.Ala97Thr | |
| ENST00000636922.1:c.177+112G>A | ENSP00000490905.1:n.177+112G>A | |
| ENST00000336553.10:c.110-946G>A | ENSP00000337665.6:n.110-946G>A | |
| ENST00000346997.6:c.289G>A | ENSP00000263451.5:p.Ala97Thr | |
| ENST00000351936.10:c.289G>A | ENSP00000309878.9:p.Ala97Thr | |
| ENST00000356226.8:c.110-14066G>A | ENSP00000348559.4:n.110-14066G>A | |
| ENST00000357555.9:c.110-946G>A | ENSP00000350166.5:n.110-946G>A | |
| ENST00000358487.9:c.289G>A | ENSP00000351276.5:p.Ala97Thr | |
| ENST00000359354.6:c.289G>A | ENSP00000352309.2:p.Ala97Thr | |
| ENST00000360144.7:c.110-946G>A | ENSP00000353262.3:n.110-946G>A | |
| ENST00000369056.5:c.289G>A | ENSP00000358052.1:p.Ala97Thr | |
| ENST00000369058.7:c.289G>A | ENSP00000358054.3:p.Ala97Thr | |
| ENST00000369059.5:c.110-14066G>A | ENSP00000358055.1:n.110-14066G>A | |
| ENST00000369060.8:c.289G>A | ENSP00000358056.4:p.Ala97Thr | |
| ENST00000369061.8:c.289G>A | ENSP00000358057.4:p.Ala97Thr | |
| ENST00000457416.6:c.289G>A | ENSP00000410294.2:p.Ala97Thr | |
| ENST00000490349.5:n.550G>A | ||
| ENST00000491475.1:n.387G>A | ||
| ENST00000604236.5:c.110-14066G>A | ENSP00000474109.1:n.110-14066G>A | |
| ENST00000611527.1:c.110-946G>A | ENSP00000484892.1:n.110-946G>A | |
| ENST00000613048.4:c.110-946G>A | ENSP00000484154.1:n.110-946G>A | |
| ENST00000613324.4:c.236G>A | ||
| NM_000141.4:c.289G>A | NP_000132.3:p.Ala97Thr | |
| NM_001144913.1:c.289G>A | NP_001138385.1:p.Ala97Thr | |
| NM_001144914.1:c.289G>A | NP_001138386.1:p.Ala97Thr | |
| NM_001144915.1:c.110-946G>A | NP_001138387.1:n.110-946G>A | |
| NM_001144916.1:c.110-14066G>A | NP_001138388.1:n.110-14066G>A | |
| NM_001144917.1:c.289G>A | NP_001138389.1:p.Ala97Thr | |
| NM_001144918.1:c.110-14066G>A | NP_001138390.1:n.110-14066G>A | |
| NM_001144919.1:c.110-946G>A | NP_001138391.1:n.110-946G>A | |
| NM_022970.3:c.289G>A | NP_075259.4:p.Ala97Thr | |
| NM_023029.2:c.110-946G>A | NP_075418.1:n.110-946G>A | |
| NR_073009.1:n.757-14066G>A | ||
| XM_006717708.2:c.346G>A | XP_006717771.1:p.Ala116Thr | |
| XM_006717709.2:c.346G>A | XP_006717772.1:p.Ala116Thr | |
| XM_006717710.2:c.346G>A | XP_006717773.1:p.Ala116Thr | |
| XM_006717711.2:c.167-946G>A | XP_006717774.1:n.167-946G>A | |
| XM_006717712.2:c.167-14066G>A | XP_006717775.1:n.167-14066G>A | |
| XM_006717713.2:c.346G>A | XP_006717776.1:p.Ala116Thr | |
| NM_001320658.1:c.289G>A | NP_001307587.1:p.Ala97Thr | |
| XM_006717708.3:c.346G>A | XP_006717771.1:p.Ala116Thr | |
| XM_006717710.4:c.346G>A | XP_006717773.1:p.Ala116Thr | |
| XM_017015920.2:c.346G>A | XP_016871409.1:p.Ala116Thr | |
| XM_017015921.2:c.346G>A | XP_016871410.1:p.Ala116Thr | |
| XM_017015924.2:c.167-14066G>A | XP_016871413.1:n.167-14066G>A | |
| XM_017015925.2:c.167-14066G>A | XP_016871414.1:n.167-14066G>A | |
| XM_024447887.1:c.167-946G>A | XP_024303655.1:n.167-946G>A | |
| XM_024447888.1:c.167-946G>A | XP_024303656.1:n.167-946G>A | |
| XM_024447889.1:c.167-946G>A | XP_024303657.1:n.167-946G>A | |
| XM_024447890.1:c.167-946G>A | XP_024303658.1:n.167-946G>A | |
| XM_024447891.1:c.167-14066G>A | XP_024303659.1:n.167-14066G>A | |
| NM_000141.5:c.289G>A MANE Select | NP_000132.3:p.Ala97Thr | |
| NM_001144917.2:c.289G>A | NP_001138389.1:p.Ala97Thr | |
| NM_001144918.2:c.110-14066G>A | NP_001138390.1:n.110-14066G>A | |
| NM_001144919.2:c.110-946G>A | NP_001138391.1:n.110-946G>A | |
| NM_001320658.2:c.289G>A | NP_001307587.1:p.Ala97Thr | |
| NR_073009.2:n.743-14066G>A | ||
| NM_001144915.2:c.110-946G>A | NP_001138387.1:n.110-946G>A | |
| NM_001144916.2:c.110-14066G>A | NP_001138388.1:n.110-14066G>A |