Linked Data
dbSNP Id:
rs1235852657
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928866A>G , CM000684.2:g.43928866A>G | GRCh38 |
| NC_000022.10:g.44324746A>G , CM000684.1:g.44324746A>G | GRCh37 |
| NC_000022.9:g.42656079A>G | NCBI36 |
| NG_008631.1:g.10128A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.463A>G MANE Select | ENSP00000216180.3:p.Ile155Val | |
| ENST00000216180.7:c.463A>G | ENSP00000216180.3:p.Ile155Val | |
| ENST00000406117.6:c.*95A>G | ENSP00000384668.2:n.*95A>G | |
| ENST00000423180.2:c.451A>G | ENSP00000397987.2:p.Ile151Val | |
| ENST00000478713.1:n.497A>G | ||
| NM_025225.2:c.463A>G | NP_079501.2:p.Ile155Val | |
| NM_025225.3:c.463A>G MANE Select | NP_079501.2:p.Ile155Val |