Linked Data
ClinVar Variation Id:
433448
ClinVar RCV Id:
RCV000499114
dbSNP Id:
rs368017088
gnomAD v2:
16-16284137-C-A
gnomAD v4:
16-16190280-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16190280C>A , CM000678.2:g.16190280C>A | GRCh38 |
| NC_000016.9:g.16284137C>A , CM000678.1:g.16284137C>A | GRCh37 |
| NC_000016.8:g.16191638C>A | NCBI36 |
| NG_007558.2:g.38192G>T | |
| NG_007558.3:g.38338G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.1519G>T | ENSP00000483331.2:p.Glu507Ter | |
| ENST00000205557.12:c.1519G>T MANE Select | ENSP00000205557.7:p.Glu507Ter | |
| ENST00000205557.11:c.1519G>T | ENSP00000205557.7:p.Glu507Ter | |
| ENST00000456970.6:c.1519G>T | ENSP00000405002.2:p.Glu507Ter | |
| ENST00000574094.5:n.1615G>T | ||
| ENST00000622290.4:c.1519G>T | ENSP00000483331.1:p.Glu507Ter | |
| NM_001171.5:c.1519G>T | NP_001162.4:p.Glu507Ter | |
| XM_011522479.1:c.1519G>T | XP_011520781.1:p.Glu507Ter | |
| XM_011522480.1:c.1177G>T | XP_011520782.1:p.Glu393Ter | |
| XM_011522481.1:c.1177G>T | XP_011520783.1:p.Glu393Ter | |
| XM_011522482.1:c.1519G>T | XP_011520784.1:p.Glu507Ter | |
| XR_932836.1:n.1754G>T | ||
| XR_932837.1:n.1755G>T | ||
| XR_932838.1:n.1755G>T | ||
| NM_001351800.1:c.1177G>T | NP_001338729.1:p.Glu393Ter | |
| NR_147784.1:n.1556G>T | ||
| XM_011522479.2:c.1519G>T | XP_011520781.1:p.Glu507Ter | |
| XM_011522481.3:c.1177G>T | XP_011520783.1:p.Glu393Ter | |
| XM_011522482.3:c.1519G>T | XP_011520784.1:p.Glu507Ter | |
| XM_017023212.1:c.1519G>T | XP_016878701.1:p.Glu507Ter | |
| XM_017023214.1:c.1519G>T | XP_016878703.1:p.Glu507Ter | |
| XM_024450261.1:c.1555G>T | XP_024306029.1:p.Glu519Ter | |
| XR_932836.2:n.1700G>T | ||
| XR_932837.3:n.1700G>T | ||
| XR_932838.3:n.1700G>T | ||
| NM_001171.6:c.1519G>T MANE Select | NP_001162.5:p.Glu507Ter |