MyVariant.info:
GRCh37
chr16:g.14041607C>G
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13947750C>G , CM000678.2:g.13947750C>G | GRCh38 |
| NC_000016.9:g.14041607C>G , CM000678.1:g.14041607C>G | GRCh37 |
| NC_000016.8:g.13949108C>G | NCBI36 |
| NG_011442.1:g.32594C>G , LRG_463:g.32594C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2292C>G | ENSP00000507912.1:p.Leu764= | |
| ENST00000683962.1:c.*1848C>G | ENSP00000506854.1:n.*1848C>G | |
| ENST00000311895.8:c.2154C>G MANE Select | ENSP00000310520.7:p.Leu718= | |
| ENST00000311895.7:c.2154C>G | ENSP00000310520.7:p.Leu718= | |
| ENST00000389138.7:n.1431C>G | ||
| ENST00000462862.1:c.467C>G | ENSP00000461322.1:n.467C>G | |
| NM_005236.2:c.2154C>G , LRG_463t1:c.2154C>G | NP_005227.1:p.Leu718= | |
| XM_011522424.1:c.2292C>G | XP_011520726.1:p.Leu764= | |
| XM_011522425.1:c.1611C>G | XP_011520727.1:p.Leu537= | |
| XM_011522426.1:c.1365C>G | XP_011520728.1:p.Leu455= | |
| XM_011522427.1:c.804C>G | XP_011520729.1:p.Leu268= | |
| XR_932805.1:n.2313C>G | ||
| XM_011522424.3:c.2292C>G | XP_011520726.1:p.Leu764= | |
| XM_017023043.2:c.1365C>G | XP_016878532.1:p.Leu455= | |
| NM_005236.3:c.2154C>G MANE Select | NP_005227.1:p.Leu718= |