Linked Data
dbSNP Id:
rs1350234938
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745740A>G , CM000665.2:g.8745740A>G | GRCh38 |
| NC_000003.11:g.8787426A>G , CM000665.1:g.8787426A>G | GRCh37 |
| NC_000003.10:g.8762426A>G | NCBI36 |
| NG_008797.2:g.16931A>G , LRG_329:g.16931A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343849.3:c.329A>G MANE Select | ENSP00000341940.2:p.Tyr110Cys | |
| ENST00000343849.2:c.329A>G | ENSP00000341940.2:p.Tyr110Cys | |
| ENST00000397368.2:c.329A>G | ENSP00000380525.2:p.Tyr110Cys | |
| ENST00000472766.1:n.155+11750A>G | ||
| NM_001234.4:c.329A>G | NP_001225.1:p.Tyr110Cys | |
| NM_033337.2:c.329A>G , LRG_329t1:c.329A>G | NP_203123.1:p.Tyr110Cys | |
| NM_001234.5:c.329A>G | NP_001225.1:p.Tyr110Cys | |
| NM_033337.3:c.329A>G MANE Select | NP_203123.1:p.Tyr110Cys |