Linked Data
MyVariant Identifiers:
chr1:g.160098579C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160128789C>G , CM000663.2:g.160128789C>G | GRCh38 |
| NC_000001.10:g.160098579C>G , CM000663.1:g.160098579C>G | GRCh37 |
| NC_000001.9:g.158365203C>G | NCBI36 |
| NG_008014.1:g.18032C>G , LRG_6:g.18032C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.1155C>G MANE Select | ENSP00000354490.3:p.Thr385= | |
| ENST00000361216.7:c.1155C>G | ENSP00000354490.3:p.Thr385= | |
| ENST00000392233.7:c.1155C>G | ENSP00000376066.3:p.Thr385= | |
| ENST00000447527.1:c.287C>G | ||
| ENST00000472488.5:n.1258C>G | ||
| NM_000702.3:c.1155C>G | NP_000693.1:p.Thr385= | |
| NM_000702.4:c.1155C>G MANE Select | NP_000693.1:p.Thr385= |