Linked Data
MyVariant Identifiers:
chr20:g.56140599G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57565543G>T , CM000682.2:g.57565543G>T | GRCh38 |
| NC_000020.10:g.56140599G>T , CM000682.1:g.56140599G>T | GRCh37 |
| NC_000020.9:g.55574005G>T | NCBI36 |
| NG_008205.1:g.9463G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.1608G>T MANE Select | ENSP00000319814.4:p.Val536= | |
| ENST00000319441.5:c.1608G>T | ENSP00000319814.4:p.Val536= | |
| ENST00000467047.1:n.4250G>T | ||
| NM_002591.3:c.1608G>T | NP_002582.3:p.Val536= | |
| XM_011528839.1:c.1212G>T | XP_011527141.1:p.Val404= | |
| XM_024451888.1:c.1212G>T | XP_024307656.1:p.Val404= | |
| NM_002591.4:c.1608G>T MANE Select | NP_002582.3:p.Val536= |