Linked Data
ClinVar Variation Id:
943396
ClinVar RCV Id:
RCV001213577
dbSNP Id:
rs750999717
ExAC:
16:14041999 A / T
gnomAD v2:
16-14041999-A-T
gnomAD v3:
16-13948142-A-T
gnomAD v4:
16-13948142-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13948142A>T , CM000678.2:g.13948142A>T | GRCh38 |
| NC_000016.9:g.14041999A>T , CM000678.1:g.14041999A>T | GRCh37 |
| NC_000016.8:g.13949500A>T | NCBI36 |
| NG_011442.1:g.32986A>T , LRG_463:g.32986A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682617.1:c.2684A>T | ENSP00000507912.1:p.Gln895Leu | |
| ENST00000683962.1:c.*2240A>T | ENSP00000506854.1:n.*2240A>T | |
| ENST00000311895.8:c.2546A>T MANE Select | ENSP00000310520.7:p.Gln849Leu | |
| ENST00000311895.7:c.2546A>T | ENSP00000310520.7:p.Gln849Leu | |
| ENST00000389138.7:n.1823A>T | ||
| NM_005236.2:c.2546A>T , LRG_463t1:c.2546A>T | NP_005227.1:p.Gln849Leu | |
| XM_011522424.1:c.2684A>T | XP_011520726.1:p.Gln895Leu | |
| XM_011522425.1:c.2003A>T | XP_011520727.1:p.Gln668Leu | |
| XM_011522426.1:c.1757A>T | XP_011520728.1:p.Gln586Leu | |
| XM_011522427.1:c.1196A>T | XP_011520729.1:p.Gln399Leu | |
| XR_932805.1:n.2705A>T | ||
| XM_011522424.3:c.2684A>T | XP_011520726.1:p.Gln895Leu | |
| XM_017023043.2:c.1757A>T | XP_016878532.1:p.Gln586Leu | |
| NM_005236.3:c.2546A>T MANE Select | NP_005227.1:p.Gln849Leu |