Linked Data
ClinVar Variation Id:
776985
ClinVar RCV Id:
RCV000957381
dbSNP Id:
rs146523238
ExAC:
16:16297272 C / A
gnomAD v2:
16-16297272-C-A
gnomAD v3:
16-16203415-C-A
gnomAD v4:
16-16203415-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16203415C>A , CM000678.2:g.16203415C>A | GRCh38 |
| NC_000016.9:g.16297272C>A , CM000678.1:g.16297272C>A | GRCh37 |
| NC_000016.8:g.16204773C>A | NCBI36 |
| NG_007558.2:g.25057G>T | |
| NG_007558.3:g.25203G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000574094.6:c.993G>T | ENSP00000507301.1:p.Leu331= | |
| ENST00000622290.5:c.993G>T | ENSP00000483331.2:p.Leu331= | |
| ENST00000205557.12:c.993G>T MANE Select | ENSP00000205557.7:p.Leu331= | |
| ENST00000205557.11:c.993G>T | ENSP00000205557.7:p.Leu331= | |
| ENST00000456970.6:c.993G>T | ENSP00000405002.2:p.Leu331= | |
| ENST00000574094.5:n.1089G>T | ||
| ENST00000577103.1:c.*860G>T | ENSP00000459243.1:n.*860G>T | |
| ENST00000622290.4:c.993G>T | ENSP00000483331.1:p.Leu331= | |
| NM_001171.5:c.993G>T | NP_001162.4:p.Leu331= | |
| XM_011522479.1:c.993G>T | XP_011520781.1:p.Leu331= | |
| XM_011522480.1:c.651G>T | XP_011520782.1:p.Leu217= | |
| XM_011522481.1:c.651G>T | XP_011520783.1:p.Leu217= | |
| XM_011522482.1:c.993G>T | XP_011520784.1:p.Leu331= | |
| XR_932836.1:n.1228G>T | ||
| XR_932837.1:n.1229G>T | ||
| XR_932838.1:n.1229G>T | ||
| NM_001351800.1:c.651G>T | NP_001338729.1:p.Leu217= | |
| NR_147784.1:n.1030G>T | ||
| XM_011522479.2:c.993G>T | XP_011520781.1:p.Leu331= | |
| XM_011522481.3:c.651G>T | XP_011520783.1:p.Leu217= | |
| XM_011522482.3:c.993G>T | XP_011520784.1:p.Leu331= | |
| XM_017023212.1:c.993G>T | XP_016878701.1:p.Leu331= | |
| XM_017023214.1:c.993G>T | XP_016878703.1:p.Leu331= | |
| XM_024450261.1:c.1029G>T | XP_024306029.1:p.Leu343= | |
| XR_932836.2:n.1174G>T | ||
| XR_932837.3:n.1174G>T | ||
| XR_932838.3:n.1174G>T | ||
| NM_001171.6:c.993G>T MANE Select | NP_001162.5:p.Leu331= |