Linked Data
MyVariant Identifiers:
chr1:g.160851948G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160882158G>C , CM000663.2:g.160882158G>C | GRCh38 |
| NC_000001.10:g.160851948G>C , CM000663.1:g.160851948G>C | GRCh37 |
| NC_000001.9:g.159118572G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000326245.4:c.204C>G MANE Select | ENSP00000323587.3:p.Thr68= | |
| ENST00000326245.3:c.204C>G | ENSP00000323587.3:p.Thr68= | |
| ENST00000464077.1:n.138C>G | ||
| NM_017625.2:c.204C>G | NP_060095.2:p.Thr68= | |
| NM_017625.3:c.204C>G MANE Select | NP_060095.2:p.Thr68= |