Linked Data
MyVariant Identifiers:
chr20:g.60503270C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.61928212C>G , CM000682.2:g.61928212C>G | GRCh38 |
| NC_000020.10:g.60503270C>G , CM000682.1:g.60503270C>G | GRCh37 |
| NC_000020.9:g.59936665C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614565.5:c.1794C>G MANE Select | ENSP00000484928.1:p.Thr598= | |
| ENST00000543233.2:c.1572C>G | ENSP00000443301.1:p.Thr524= | |
| ENST00000611855.4:c.1512C>G | ENSP00000480844.1:p.Thr504= | |
| ENST00000614565.4:c.1794C>G | ENSP00000484928.1:p.Thr598= | |
| NM_001252338.2:c.1683C>G | NP_001239267.1:p.Thr561= | |
| NM_001252339.2:c.1572C>G | NP_001239268.1:p.Thr524= | |
| NM_001794.4:c.1794C>G | NP_001785.2:p.Thr598= | |
| NM_001794.5:c.1794C>G MANE Select | NP_001785.2:p.Thr598= | |
| NM_001252339.3:c.1572C>G | NP_001239268.1:p.Thr524= |