Linked Data
MyVariant Identifiers:
chr1:g.94487483T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94021927T>C , CM000663.2:g.94021927T>C | GRCh38 |
| NC_000001.10:g.94487483T>C , CM000663.1:g.94487483T>C | GRCh37 |
| NC_000001.9:g.94260071T>C | NCBI36 |
| NG_009073.1:g.104223A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4692A>G MANE Select | ENSP00000359245.3:p.Gly1564= | |
| ENST00000370225.3:c.4692A>G | ENSP00000359245.3:p.Gly1564= | |
| ENST00000460514.1:n.186A>G | ||
| ENST00000536513.5:c.1068A>G | ENSP00000439707.2:p.Gly356= | |
| NM_000350.2:c.4692A>G | NP_000341.2:p.Gly1564= | |
| NM_000350.3:c.4692A>G MANE Select | NP_000341.2:p.Gly1564= |