Linked Data
MyVariant Identifiers:
chr4:g.100341753C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420596C>G , CM000666.2:g.99420596C>G | GRCh38 |
| NC_000004.11:g.100341753C>G , CM000666.1:g.100341753C>G | GRCh37 |
| NC_000004.10:g.100560776C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.762G>C MANE Select | ENSP00000414254.2:p.Leu254= | |
| ENST00000209665.8:c.798G>C | ENSP00000209665.4:p.Leu266= | |
| ENST00000437033.6:c.762G>C | ENSP00000414254.2:p.Leu254= | |
| ENST00000476959.5:c.822G>C | ENSP00000420269.1:p.Leu274= | |
| ENST00000482593.5:c.591G>C | ENSP00000420613.1:p.Leu197= | |
| NM_000673.4:c.798G>C | NP_000664.2:p.Leu266= | |
| NM_001166504.1:c.822G>C | NP_001159976.1:p.Leu274= | |
| NM_000673.7:c.762G>C MANE Select | NP_000664.3:p.Leu254= | |
| NM_001166504.2:c.822G>C | NP_001159976.1:p.Leu274= |