Linked Data
ClinVar Variation Id:
490070
dbSNP Id:
rs201368043
ExAC:
16:23646172 T / C
gnomAD v2:
16-23646172-T-C
gnomAD v3:
16-23634851-T-C
gnomAD v4:
16-23634851-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23634851T>C , CM000678.2:g.23634851T>C | GRCh38 |
| NC_000016.9:g.23646172T>C , CM000678.1:g.23646172T>C | GRCh37 |
| NC_000016.8:g.23553673T>C | NCBI36 |
| NG_007406.1:g.11507A>G , LRG_308:g.11507A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.1690+11A>G | ENSP00000460666.3:n.1690+11A>G | |
| ENST00000565038.2:c.211+2999A>G | ENSP00000459882.2:n.211+2999A>G | |
| ENST00000566069.6:c.1684+11A>G | ENSP00000459237.2:n.1684+11A>G | |
| ENST00000697377.2:c.1690+11A>G | ENSP00000513286.2:n.1690+11A>G | |
| ENST00000697379.2:c.1690+11A>G | ENSP00000513287.2:n.1690+11A>G | |
| ENST00000561514.2:c.799+11A>G | ENSP00000460666.2:n.799+11A>G | |
| ENST00000697374.1:c.799+11A>G | ENSP00000513284.1:n.799+11A>G | |
| ENST00000697375.1:n.3031+11A>G | ||
| ENST00000697376.1:c.799+11A>G | ENSP00000513285.1:n.799+11A>G | |
| ENST00000697377.1:c.799+11A>G | ENSP00000513286.1:n.799+11A>G | |
| ENST00000697378.1:n.2204+11A>G | ||
| ENST00000697379.1:c.799+11A>G | ENSP00000513287.1:n.799+11A>G | |
| ENST00000697382.1:c.799+11A>G | ENSP00000513288.1:n.799+11A>G | |
| ENST00000697383.1:c.49-5576A>G | ENSP00000513289.1:n.49-5576A>G | |
| ENST00000697384.1:n.1838+11A>G | ||
| ENST00000261584.9:c.1684+11A>G MANE Select | ENSP00000261584.4:n.1684+11A>G | |
| ENST00000261584.8:c.1684+11A>G | ENSP00000261584.4:n.1684+11A>G | |
| ENST00000565038.1:c.86+2999A>G | ||
| ENST00000568219.5:c.799+11A>G | ENSP00000454703.2:n.799+11A>G | |
| NM_024675.3:c.1684+11A>G , LRG_308t1:c.1684+11A>G | NP_078951.2:n.1684+11A>G | |
| XM_011545946.1:c.1690+11A>G | XP_011544248.1:n.1690+11A>G | |
| XM_011545947.1:c.1690+11A>G | XP_011544249.1:n.1690+11A>G | |
| XM_011545948.1:c.799+11A>G | XP_011544250.1:n.799+11A>G | |
| XR_950851.1:n.2480+11A>G | ||
| XM_011545946.2:c.1690+11A>G | XP_011544248.1:n.1690+11A>G | |
| XM_011545947.2:c.1690+11A>G | XP_011544249.1:n.1690+11A>G | |
| XM_011545948.2:c.799+11A>G | XP_011544250.1:n.799+11A>G | |
| XM_017023671.1:c.1690+11A>G | XP_016879160.1:n.1690+11A>G | |
| XM_017023672.2:c.1684+11A>G | XP_016879161.1:n.1684+11A>G | |
| XM_017023673.2:c.1684+11A>G | XP_016879162.1:n.1684+11A>G | |
| NM_024675.4:c.1684+11A>G MANE Select | NP_078951.2:n.1684+11A>G |