Linked Data
MyVariant Identifiers:
chr2:g.163124608G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.162268098G>C , CM000664.2:g.162268098G>C | GRCh38 |
| NC_000002.11:g.163124608G>C , CM000664.1:g.163124608G>C | GRCh37 |
| NC_000002.10:g.162832854G>C | NCBI36 |
| NG_011495.1:g.55432C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697291.1:c.*2393C>G | ENSP00000513228.1:n.*2393C>G | |
| ENST00000648433.1:c.2679C>G | ENSP00000496816.1:p.Thr893= | |
| ENST00000649426.1:n.40C>G | ||
| ENST00000649554.1:n.2406C>G | ||
| ENST00000649979.2:c.2796C>G MANE Select | ENSP00000497271.1:p.Thr932= | |
| ENST00000679938.1:c.2484C>G | ENSP00000505518.1:p.Thr828= | |
| ENST00000263642.2:c.2796C>G | ENSP00000263642.2:p.Thr932= | |
| NM_022168.3:c.2796C>G | NP_071451.2:p.Thr932= | |
| XM_011511628.1:c.2079C>G | XP_011509930.1:p.Thr693= | |
| NM_022168.4:c.2796C>G MANE Select | NP_071451.2:p.Thr932= |