Linked Data
MyVariant Identifiers:
chr1:g.94467486C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94001930C>G , CM000663.2:g.94001930C>G | GRCh38 |
| NC_000001.10:g.94467486C>G , CM000663.1:g.94467486C>G | GRCh37 |
| NC_000001.9:g.94240074C>G | NCBI36 |
| NG_009073.1:g.124220G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6210G>C MANE Select | ENSP00000359245.3:p.Thr2070= | |
| ENST00000370225.3:c.6210G>C | ENSP00000359245.3:p.Thr2070= | |
| ENST00000465352.1:n.626G>C | ||
| ENST00000536513.5:c.2586G>C | ENSP00000439707.2:p.Thr862= | |
| NM_000350.2:c.6210G>C | NP_000341.2:p.Thr2070= | |
| NM_000350.3:c.6210G>C MANE Select | NP_000341.2:p.Thr2070= |