Linked Data
ClinVar Variation Id:
386669
dbSNP Id:
rs374927292
ExAC:
3:10191547 C / T
gnomAD v2:
3-10191547-C-T
gnomAD v3:
3-10149863-C-T
gnomAD v4:
3-10149863-C-T
COSMIC:
COSM3584705
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10149863C>T , CM000665.2:g.10149863C>T | GRCh38 |
| NC_000003.11:g.10191547C>T , CM000665.1:g.10191547C>T | GRCh37 |
| NC_000003.10:g.10166547C>T | NCBI36 |
| NG_008212.3:g.13229C>T , LRG_322:g.13229C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*217C>T | ENSP00000512434.1:n.*217C>T | |
| ENST00000696143.1:c.676C>T | ENSP00000512435.1:n.676C>T | |
| ENST00000696153.1:c.651C>T | ENSP00000512444.1:p.Ile217= | |
| ENST00000256474.3:c.540C>T MANE Select | ENSP00000256474.3:p.Ile180= | |
| ENST00000256474.2:c.540C>T | ENSP00000256474.2:p.Ile180= | |
| ENST00000345392.2:c.417C>T | ENSP00000344757.2:p.Ile139= | |
| ENST00000477538.1:n.676C>T | ||
| NM_000551.3:c.540C>T , LRG_322t1:c.540C>T | NP_000542.1:p.Ile180= | |
| NM_198156.2:c.417C>T | NP_937799.1:p.Ile139= | |
| NM_001354723.1:c.*94C>T | NP_001341652.1:n.*94C>T | |
| NM_000551.4:c.540C>T MANE Select | NP_000542.1:p.Ile180= | |
| NM_001354723.2:c.*94C>T | NP_001341652.1:n.*94C>T | |
| NM_198156.3:c.417C>T | NP_937799.1:p.Ile139= |