Linked Data
MyVariant Identifiers:
chr12:g.103246706T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102852928T>C , CM000674.2:g.102852928T>C | GRCh38 |
| NC_000012.11:g.103246706T>C , CM000674.1:g.103246706T>C | GRCh37 |
| NC_000012.10:g.101770836T>C | NCBI36 |
| NG_008690.1:g.69675A>G | |
| NG_008690.2:g.110483A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.729A>G MANE Select | ENSP00000448059.1:p.Arg243= | |
| ENST00000307000.7:c.714A>G | ENSP00000303500.2:p.Arg238= | |
| ENST00000549247.6:n.488A>G | ||
| ENST00000553106.5:c.729A>G | ENSP00000448059.1:p.Arg243= | |
| NM_000277.1:c.729A>G | NP_000268.1:p.Arg243= | |
| XM_011538422.1:c.729A>G | XP_011536724.1:p.Arg243= | |
| NM_000277.2:c.729A>G | NP_000268.1:p.Arg243= | |
| NM_001354304.1:c.729A>G | NP_001341233.1:p.Arg243= | |
| NM_000277.3:c.729A>G MANE Select | NP_000268.1:p.Arg243= | |
| NM_001354304.2:c.729A>G | NP_001341233.1:p.Arg243= |