Linked Data
ClinVar Variation Id:
1732878
dbSNP Id:
rs1575477934
MyVariant Identifiers:
chr3:g.8787454C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745768C>T , CM000665.2:g.8745768C>T | GRCh38 |
| NC_000003.11:g.8787454C>T , CM000665.1:g.8787454C>T | GRCh37 |
| NC_000003.10:g.8762454C>T | NCBI36 |
| NG_008797.2:g.16959C>T , LRG_329:g.16959C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343849.3:c.357C>T MANE Select | ENSP00000341940.2:p.His119= | |
| ENST00000343849.2:c.357C>T | ENSP00000341940.2:p.His119= | |
| ENST00000397368.2:c.357C>T | ENSP00000380525.2:p.His119= | |
| ENST00000472766.1:n.155+11778C>T | ||
| NM_001234.4:c.357C>T | NP_001225.1:p.His119= | |
| NM_033337.2:c.357C>T , LRG_329t1:c.357C>T | NP_203123.1:p.His119= | |
| NM_001234.5:c.357C>T | NP_001225.1:p.His119= | |
| NM_033337.3:c.357C>T MANE Select | NP_203123.1:p.His119= |