Linked Data
MyVariant Identifiers:
chr20:g.56137942T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562886T>G , CM000682.2:g.57562886T>G | GRCh38 |
| NC_000020.10:g.56137942T>G , CM000682.1:g.56137942T>G | GRCh37 |
| NC_000020.9:g.55571348T>G | NCBI36 |
| NG_008205.1:g.6806T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.597T>G MANE Select | ENSP00000319814.4:p.Pro199= | |
| ENST00000319441.5:c.597T>G | ENSP00000319814.4:p.Pro199= | |
| ENST00000467047.1:n.1807T>G | ||
| ENST00000470051.1:n.53T>G | ||
| ENST00000498194.1:n.539T>G | ||
| NM_002591.3:c.597T>G | NP_002582.3:p.Pro199= | |
| XM_011528839.1:c.201T>G | XP_011527141.1:p.Pro67= | |
| XM_024451888.1:c.201T>G | XP_024307656.1:p.Pro67= | |
| NM_002591.4:c.597T>G MANE Select | NP_002582.3:p.Pro199= |