Linked Data
MyVariant Identifiers:
chr4:g.100341777A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420620A>C , CM000666.2:g.99420620A>C | GRCh38 |
| NC_000004.11:g.100341777A>C , CM000666.1:g.100341777A>C | GRCh37 |
| NC_000004.10:g.100560800A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.738T>G MANE Select | ENSP00000414254.2:p.Ser246= | |
| ENST00000209665.8:c.774T>G | ENSP00000209665.4:p.Ser258= | |
| ENST00000437033.6:c.738T>G | ENSP00000414254.2:p.Ser246= | |
| ENST00000476959.5:c.798T>G | ENSP00000420269.1:p.Ser266= | |
| ENST00000482593.5:c.567T>G | ENSP00000420613.1:p.Ser189= | |
| NM_000673.4:c.774T>G | NP_000664.2:p.Ser258= | |
| NM_001166504.1:c.798T>G | NP_001159976.1:p.Ser266= | |
| NM_000673.7:c.738T>G MANE Select | NP_000664.3:p.Ser246= | |
| NM_001166504.2:c.798T>G | NP_001159976.1:p.Ser266= |