Linked Data
dbSNP Id:
rs778151578
ExAC:
16:16263568 A / T
gnomAD v2:
16-16263568-A-T
gnomAD v4:
16-16169711-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16169711A>T , CM000678.2:g.16169711A>T | GRCh38 |
| NC_000016.9:g.16263568A>T , CM000678.1:g.16263568A>T | GRCh37 |
| NC_000016.8:g.16171069A>T | NCBI36 |
| NG_007558.2:g.58761T>A | |
| NG_007558.3:g.58907T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.2930T>A | ENSP00000483331.2:p.Val977Glu | |
| ENST00000205557.12:c.2930T>A MANE Select | ENSP00000205557.7:p.Val977Glu | |
| ENST00000205557.11:c.2930T>A | ENSP00000205557.7:p.Val977Glu | |
| ENST00000456970.6:c.2755T>A | ENSP00000405002.2:n.2755T>A | |
| ENST00000622290.4:c.*139T>A | ENSP00000483331.1:n.*139T>A | |
| NM_001171.5:c.2930T>A | NP_001162.4:p.Val977Glu | |
| XM_011522479.1:c.2897T>A | XP_011520781.1:p.Val966Glu | |
| XM_011522480.1:c.2588T>A | XP_011520782.1:p.Val863Glu | |
| XM_011522481.1:c.2588T>A | XP_011520783.1:p.Val863Glu | |
| XR_932836.1:n.3165T>A | ||
| XR_932837.1:n.3166T>A | ||
| XR_932838.1:n.3166T>A | ||
| NM_001351800.1:c.2588T>A | NP_001338729.1:p.Val863Glu | |
| NR_147784.1:n.2792T>A | ||
| XM_011522479.2:c.2897T>A | XP_011520781.1:p.Val966Glu | |
| XM_011522481.3:c.2588T>A | XP_011520783.1:p.Val863Glu | |
| XM_017023212.1:c.2762T>A | XP_016878701.1:p.Val921Glu | |
| XM_017023214.1:c.2930T>A | XP_016878703.1:p.Val977Glu | |
| XM_024450261.1:c.2966T>A | XP_024306029.1:p.Val989Glu | |
| XR_932836.2:n.3111T>A | ||
| XR_932837.3:n.3111T>A | ||
| XR_932838.3:n.3111T>A | ||
| NM_001171.6:c.2930T>A MANE Select | NP_001162.5:p.Val977Glu |