Linked Data
MyVariant Identifiers:
chr20:g.10393389T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10412741T>C , CM000682.2:g.10412741T>C | GRCh38 |
| NC_000020.10:g.10393389T>C , CM000682.1:g.10393389T>C | GRCh37 |
| NC_000020.9:g.10341389T>C | NCBI36 |
| NG_009109.1:g.26478A>G | |
| NG_009109.2:g.26478A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651692.1:c.774A>G | ENSP00000498849.1:p.Gly258= | |
| ENST00000652676.1:n.459-41A>G | ||
| ENST00000347364.7:c.774A>G MANE Select | ENSP00000246062.4:p.Gly258= | |
| ENST00000399054.6:c.774A>G | ENSP00000382008.2:p.Gly258= | |
| NM_018848.3:c.774A>G | NP_061336.1:p.Gly258= | |
| NM_170784.2:c.774A>G | NP_740754.1:p.Gly258= | |
| NR_072977.1:n.364-3938A>G | ||
| NR_072977.2:n.347-3938A>G | ||
| NM_170784.3:c.774A>G MANE Select | NP_740754.1:p.Gly258= |