Linked Data
ClinVar Variation Id:
291552
dbSNP Id:
rs142881321
ExAC:
1:10357048 C / T
gnomAD v2:
1-10357048-C-T
gnomAD v3:
1-10296990-C-T
gnomAD v4:
1-10296990-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.10296990C>T , CM000663.2:g.10296990C>T | GRCh38 |
| NC_000001.10:g.10357048C>T , CM000663.1:g.10357048C>T | GRCh37 |
| NC_000001.9:g.10279635C>T | NCBI36 |
| NG_008069.1:g.91285C>T , LRG_252:g.91285C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696500.1:c.*989C>T | ENSP00000512666.1:n.*989C>T | |
| ENST00000696502.1:c.1817C>T | ENSP00000512668.1:p.Thr606Ile | |
| ENST00000696503.1:c.1880C>T | ENSP00000512669.1:p.Thr627Ile | |
| ENST00000696504.1:c.1880C>T | ENSP00000512670.1:p.Thr627Ile | |
| ENST00000377093.9:c.1817C>T | ENSP00000366297.4:p.Thr606Ile | |
| ENST00000676179.1:c.1955C>T MANE Select | ENSP00000502065.1:p.Thr652Ile | |
| ENST00000263934.10:c.1817C>T | ENSP00000263934.6:p.Thr606Ile | |
| ENST00000377081.5:c.1955C>T | ENSP00000366284.1:p.Thr652Ile | |
| ENST00000377083.5:c.1817C>T | ENSP00000366287.1:p.Thr606Ile | |
| ENST00000377086.5:c.1955C>T | ENSP00000366290.1:p.Thr652Ile | |
| ENST00000377093.8:c.1817C>T | ENSP00000366297.4:p.Thr606Ile | |
| ENST00000620295.2:c.1913C>T | ENSP00000478500.1:p.Thr638Ile | |
| ENST00000622724.3:c.1877C>T | ENSP00000480063.1:p.Thr626Ile | |
| NM_015074.3:c.1817C>T , LRG_252t1:c.1817C>T | NP_055889.2:p.Thr606Ile | |
| NM_183416.3:c.1817C>T | NP_904325.2:p.Thr606Ile | |
| NM_001365951.1:c.1955C>T | NP_001352880.1:p.Thr652Ile | |
| NM_001365952.1:c.1955C>T | NP_001352881.1:p.Thr652Ile | |
| NM_001365953.1:c.1817C>T | NP_001352882.1:p.Thr606Ile | |
| NM_001365951.3:c.1955C>T MANE Select | NP_001352880.1:p.Thr652Ile | |
| NM_183416.4:c.1817C>T | NP_904325.2:p.Thr606Ile |