Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562831T>A , CM000682.2:g.57562831T>A | GRCh38 |
| NC_000020.10:g.56137887T>A , CM000682.1:g.56137887T>A | GRCh37 |
| NC_000020.9:g.55571293T>A | NCBI36 |
| NG_008205.1:g.6751T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.542T>A MANE Select | ENSP00000319814.4:p.Leu181Gln | |
| ENST00000319441.5:c.542T>A | ENSP00000319814.4:p.Leu181Gln | |
| ENST00000467047.1:n.1752T>A | ||
| ENST00000498194.1:n.484T>A | ||
| NM_002591.3:c.542T>A | NP_002582.3:p.Leu181Gln | |
| XM_011528839.1:c.146T>A | XP_011527141.1:p.Leu49Gln | |
| XM_024451888.1:c.146T>A | XP_024307656.1:p.Leu49Gln | |
| NM_002591.4:c.542T>A MANE Select | NP_002582.3:p.Leu181Gln |