MyVariant.info:
GRCh37
chr12:g.103246637T>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102852859T>G , CM000674.2:g.102852859T>G | GRCh38 |
| NC_000012.11:g.103246637T>G , CM000674.1:g.103246637T>G | GRCh37 |
| NC_000012.10:g.101770767T>G | NCBI36 |
| NG_008690.1:g.69744A>C | |
| NG_008690.2:g.110552A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.798A>C MANE Select | ENSP00000448059.1:p.Thr266= | |
| ENST00000307000.7:c.783A>C | ENSP00000303500.2:p.Thr261= | |
| ENST00000549247.6:n.557A>C | ||
| ENST00000553106.5:c.798A>C | ENSP00000448059.1:p.Thr266= | |
| NM_000277.1:c.798A>C | NP_000268.1:p.Thr266= | |
| XM_011538422.1:c.798A>C | XP_011536724.1:p.Thr266= | |
| NM_000277.2:c.798A>C | NP_000268.1:p.Thr266= | |
| NM_001354304.1:c.798A>C | NP_001341233.1:p.Thr266= | |
| NM_000277.3:c.798A>C MANE Select | NP_000268.1:p.Thr266= | |
| NM_001354304.2:c.798A>C | NP_001341233.1:p.Thr266= |