Linked Data
ClinVar Variation Id:
216742
ClinVar RCV Id:
RCV000200861
RCV000255070
RCV000562823
RCV000761148
RCV001194137
RCV002492922
RCV004530198
dbSNP Id:
rs146434474
ExAC:
16:23646530 T / A
gnomAD v2:
16-23646530-T-A
gnomAD v3:
16-23635209-T-A
gnomAD v4:
16-23635209-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23635209T>A , CM000678.2:g.23635209T>A | GRCh38 |
| NC_000016.9:g.23646530T>A , CM000678.1:g.23646530T>A | GRCh37 |
| NC_000016.8:g.23554031T>A | NCBI36 |
| NG_007406.1:g.11149A>T , LRG_308:g.11149A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.1343A>T | ENSP00000460666.3:p.Asp448Val | |
| ENST00000565038.2:c.211+2641A>T | ENSP00000459882.2:n.211+2641A>T | |
| ENST00000566069.6:c.1337A>T | ENSP00000459237.2:p.Asp446Val | |
| ENST00000697377.2:c.1343A>T | ENSP00000513286.2:p.Asp448Val | |
| ENST00000697379.2:c.1343A>T | ENSP00000513287.2:p.Asp448Val | |
| ENST00000561514.2:c.452A>T | ENSP00000460666.2:p.Asp151Val | |
| ENST00000697374.1:c.452A>T | ENSP00000513284.1:p.Asp151Val | |
| ENST00000697375.1:n.2684A>T | ||
| ENST00000697376.1:c.452A>T | ENSP00000513285.1:p.Asp151Val | |
| ENST00000697377.1:c.452A>T | ENSP00000513286.1:p.Asp151Val | |
| ENST00000697378.1:n.1857A>T | ||
| ENST00000697379.1:c.452A>T | ENSP00000513287.1:p.Asp151Val | |
| ENST00000697382.1:c.452A>T | ENSP00000513288.1:p.Asp151Val | |
| ENST00000697383.1:c.48+5901A>T | ENSP00000513289.1:n.48+5901A>T | |
| ENST00000697384.1:n.1491A>T | ||
| ENST00000261584.9:c.1337A>T MANE Select | ENSP00000261584.4:p.Asp446Val | |
| ENST00000261584.8:c.1337A>T | ENSP00000261584.4:p.Asp446Val | |
| ENST00000565038.1:c.86+2641A>T | ||
| ENST00000568219.5:c.452A>T | ENSP00000454703.2:p.Asp151Val | |
| NM_024675.3:c.1337A>T , LRG_308t1:c.1337A>T | NP_078951.2:p.Asp446Val | |
| XM_011545946.1:c.1343A>T | XP_011544248.1:p.Asp448Val | |
| XM_011545947.1:c.1343A>T | XP_011544249.1:p.Asp448Val | |
| XM_011545948.1:c.452A>T | XP_011544250.1:p.Asp151Val | |
| XR_950851.1:n.2133A>T | ||
| XM_011545946.2:c.1343A>T | XP_011544248.1:p.Asp448Val | |
| XM_011545947.2:c.1343A>T | XP_011544249.1:p.Asp448Val | |
| XM_011545948.2:c.452A>T | XP_011544250.1:p.Asp151Val | |
| XM_017023671.1:c.1343A>T | XP_016879160.1:p.Asp448Val | |
| XM_017023672.2:c.1337A>T | XP_016879161.1:p.Asp446Val | |
| XM_017023673.2:c.1337A>T | XP_016879162.1:p.Asp446Val | |
| NM_024675.4:c.1337A>T MANE Select | NP_078951.2:p.Asp446Val |