Linked Data
MyVariant Identifiers:
chr20:g.56140533C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57565477C>G , CM000682.2:g.57565477C>G | GRCh38 |
| NC_000020.10:g.56140533C>G , CM000682.1:g.56140533C>G | GRCh37 |
| NC_000020.9:g.55573939C>G | NCBI36 |
| NG_008205.1:g.9397C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.1542C>G MANE Select | ENSP00000319814.4:p.Val514= | |
| ENST00000319441.5:c.1542C>G | ENSP00000319814.4:p.Val514= | |
| ENST00000467047.1:n.4184C>G | ||
| NM_002591.3:c.1542C>G | NP_002582.3:p.Val514= | |
| XM_011528839.1:c.1146C>G | XP_011527141.1:p.Val382= | |
| XM_024451888.1:c.1146C>G | XP_024307656.1:p.Val382= | |
| NM_002591.4:c.1542C>G MANE Select | NP_002582.3:p.Val514= |