Linked Data
MyVariant Identifiers:
chr4:g.100341912T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420755T>C , CM000666.2:g.99420755T>C | GRCh38 |
| NC_000004.11:g.100341912T>C , CM000666.1:g.100341912T>C | GRCh37 |
| NC_000004.10:g.100560935T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.603A>G MANE Select | ENSP00000414254.2:p.Gly201= | |
| ENST00000209665.8:c.639A>G | ENSP00000209665.4:p.Gly213= | |
| ENST00000437033.6:c.603A>G | ENSP00000414254.2:p.Gly201= | |
| ENST00000476959.5:c.663A>G | ENSP00000420269.1:p.Gly221= | |
| ENST00000482593.5:c.432A>G | ENSP00000420613.1:p.Gly144= | |
| NM_000673.4:c.639A>G | NP_000664.2:p.Gly213= | |
| NM_001166504.1:c.663A>G | NP_001159976.1:p.Gly221= | |
| NM_000673.7:c.603A>G MANE Select | NP_000664.3:p.Gly201= | |
| NM_001166504.2:c.663A>G | NP_001159976.1:p.Gly221= |