Linked Data
ClinVar Variation Id:
2897472
ClinVar RCV Id:
RCV003648861
MyVariant Identifiers:
chr3:g.8787343C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745657C>G , CM000665.2:g.8745657C>G | GRCh38 |
| NC_000003.11:g.8787343C>G , CM000665.1:g.8787343C>G | GRCh37 |
| NC_000003.10:g.8762343C>G | NCBI36 |
| NG_008797.2:g.16848C>G , LRG_329:g.16848C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343849.3:c.246C>G MANE Select | ENSP00000341940.2:p.Val82= | |
| ENST00000343849.2:c.246C>G | ENSP00000341940.2:p.Val82= | |
| ENST00000397368.2:c.246C>G | ENSP00000380525.2:p.Val82= | |
| ENST00000472766.1:n.155+11667C>G | ||
| NM_001234.4:c.246C>G | NP_001225.1:p.Val82= | |
| NM_033337.2:c.246C>G , LRG_329t1:c.246C>G | NP_203123.1:p.Val82= | |
| NM_001234.5:c.246C>G | NP_001225.1:p.Val82= | |
| NM_033337.3:c.246C>G MANE Select | NP_203123.1:p.Val82= |