Linked Data
ClinVar Variation Id:
355556
dbSNP Id:
rs886061127
gnomAD v2:
6-137524658-G-A
gnomAD v3:
6-137203521-G-A
gnomAD v4:
6-137203521-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.137203521G>A , CM000668.2:g.137203521G>A | GRCh38 |
| NC_000006.11:g.137524658G>A , CM000668.1:g.137524658G>A | GRCh37 |
| NC_000006.10:g.137566351G>A | NCBI36 |
| NG_007394.1:g.20910C>T , LRG_66:g.20910C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000414770.6:c.681C>T | ENSP00000394230.2:p.Thr227= | |
| ENST00000458076.6:c.609C>T | ENSP00000389249.2:p.Thr203= | |
| ENST00000696693.1:c.588C>T | ENSP00000512814.1:p.Thr196= | |
| ENST00000696694.1:c.711C>T | ENSP00000512815.1:p.Thr237= | |
| ENST00000696695.1:c.699+12C>T | ENSP00000512816.1:n.699+12C>T | |
| ENST00000696696.1:c.*610C>T | ENSP00000512817.1:n.*610C>T | |
| ENST00000696697.1:c.657C>T | ENSP00000512818.1:p.Thr219= | |
| ENST00000696698.1:c.*165C>T | ENSP00000512819.1:n.*165C>T | |
| ENST00000367739.9:c.711C>T MANE Select | ENSP00000356713.5:p.Thr237= | |
| ENST00000642390.1:c.654C>T | ENSP00000496468.1:p.Thr218= | |
| ENST00000643119.1:c.831C>T | ENSP00000495934.1:n.831C>T | |
| ENST00000644894.1:c.588C>T | ENSP00000495272.1:p.Thr196= | |
| ENST00000645045.1:c.820C>T | ||
| ENST00000645753.1:c.588C>T | ENSP00000495103.1:p.Thr196= | |
| ENST00000646036.1:c.681C>T | ENSP00000496387.1:p.Thr227= | |
| ENST00000646898.1:c.681C>T | ENSP00000494069.1:p.Thr227= | |
| ENST00000647124.1:c.588C>T | ENSP00000496549.1:p.Thr196= | |
| ENST00000367739.8:c.711C>T | ENSP00000356713.4:p.Thr237= | |
| ENST00000458076.5:c.609C>T | ENSP00000389249.1:p.Thr203= | |
| ENST00000543628.5:c.711C>T | ENSP00000443282.2:p.Thr237= | |
| NM_000416.2:c.711C>T , LRG_66t1:c.711C>T | NP_000407.1:p.Thr237= | |
| XM_006715470.2:c.681C>T | XP_006715533.1:p.Thr227= | |
| XM_006715471.2:c.588C>T | XP_006715534.1:p.Thr196= | |
| XM_011535793.1:c.681C>T | XP_011534095.1:p.Thr227= | |
| XM_011535794.1:c.681C>T | XP_011534096.1:p.Thr227= | |
| NM_001363526.1:c.681C>T | NP_001350455.1:p.Thr227= | |
| NM_001363527.1:c.588C>T | NP_001350456.1:p.Thr196= | |
| XM_006715470.3:c.681C>T | XP_006715533.1:p.Thr227= | |
| XM_011535793.2:c.681C>T | XP_011534095.1:p.Thr227= | |
| NM_000416.3:c.711C>T MANE Select | NP_000407.1:p.Thr237= |