Linked Data
MyVariant Identifiers:
chr4:g.100341726T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420569T>C , CM000666.2:g.99420569T>C | GRCh38 |
| NC_000004.11:g.100341726T>C , CM000666.1:g.100341726T>C | GRCh37 |
| NC_000004.10:g.100560749T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.789A>G MANE Select | ENSP00000414254.2:p.Gly263= | |
| ENST00000209665.8:c.825A>G | ENSP00000209665.4:p.Gly275= | |
| ENST00000437033.6:c.789A>G | ENSP00000414254.2:p.Gly263= | |
| ENST00000476959.5:c.849A>G | ENSP00000420269.1:p.Gly283= | |
| ENST00000482593.5:c.618A>G | ENSP00000420613.1:p.Gly206= | |
| NM_000673.4:c.825A>G | NP_000664.2:p.Gly275= | |
| NM_001166504.1:c.849A>G | NP_001159976.1:p.Gly283= | |
| NM_000673.7:c.789A>G MANE Select | NP_000664.3:p.Gly263= | |
| NM_001166504.2:c.849A>G | NP_001159976.1:p.Gly283= |