Linked Data
MyVariant Identifiers:
chr1:g.160851780T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160881990T>G , CM000663.2:g.160881990T>G | GRCh38 |
| NC_000001.10:g.160851780T>G , CM000663.1:g.160851780T>G | GRCh37 |
| NC_000001.9:g.159118404T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326245.4:c.372A>C MANE Select | ENSP00000323587.3:p.Gly124= | |
| ENST00000326245.3:c.372A>C | ENSP00000323587.3:p.Gly124= | |
| ENST00000464077.1:n.306A>C | ||
| NM_017625.2:c.372A>C | NP_060095.2:p.Gly124= | |
| NM_017625.3:c.372A>C MANE Select | NP_060095.2:p.Gly124= |