Linked Data
MyVariant Identifiers:
chr4:g.68797716T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67931998T>C , CM000666.2:g.67931998T>C | GRCh38 |
| NC_000004.11:g.68797716T>C , CM000666.1:g.68797716T>C | GRCh37 |
| NC_000004.10:g.68480311T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508048.6:c.315A>G MANE Select | ENSP00000426911.2:p.Arg105= | |
| ENST00000334830.11:c.324A>G | ENSP00000334611.7:p.Arg108= | |
| ENST00000396188.3:c.315A>G | ENSP00000379491.3:p.Arg105= | |
| ENST00000508048.5:c.315A>G | ENSP00000426911.2:p.Arg105= | |
| ENST00000513536.5:c.255A>G | ENSP00000427621.1:p.Arg85= | |
| NM_001114387.1:c.315A>G | NP_001107859.1:p.Arg105= | |
| NM_182606.3:c.324A>G | NP_872412.3:p.Arg108= | |
| NM_001114387.2:c.315A>G MANE Select | NP_001107859.1:p.Arg105= | |
| NM_182606.4:c.324A>G | NP_872412.3:p.Arg108= |