Linked Data
dbSNP Id:
rs1350332401
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71719353A>G , CM000667.2:g.71719353A>G | GRCh38 |
| NC_000005.9:g.71015180A>G , CM000667.1:g.71015180A>G | GRCh37 |
| NC_000005.8:g.71050936A>G | NCBI36 |
| NG_015988.1:g.5191A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296777.5:c.60A>G MANE Select | ENSP00000296777.4:p.Leu20= | |
| ENST00000296777.4:c.60A>G | ENSP00000296777.4:p.Leu20= | |
| NM_004291.3:c.60A>G | NP_004282.1:p.Leu20= | |
| NM_004291.4:c.60A>G MANE Select | NP_004282.1:p.Leu20= |