Linked Data
ClinVar Variation Id:
1559545
dbSNP Id:
rs755007049
ExAC:
11:32456826 A / G
gnomAD v2:
11-32456826-A-G
gnomAD v3:
11-32435280-A-G
gnomAD v4:
11-32435280-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.32435280A>G , CM000673.2:g.32435280A>G | GRCh38 |
| NC_000011.9:g.32456826A>G , CM000673.1:g.32456826A>G | GRCh37 |
| NC_000011.8:g.32413402A>G | NCBI36 |
| NG_009272.1:g.5262T>C , LRG_525:g.5262T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332351.9:c.81T>C | ENSP00000331327.5:p.Pro27= | |
| ENST00000379077.9:c.81T>C | ENSP00000368368.5:p.Pro27= | |
| ENST00000448076.9:c.81T>C | ENSP00000413452.5:p.Pro27= | |
| ENST00000452863.10:c.81T>C MANE Select | ENSP00000415516.5:p.Pro27= | |
| ENST00000639563.3:c.81T>C | ENSP00000492269.3:p.Pro27= | |
| ENST00000332351.7:c.66T>C | ENSP00000331327.3:p.Pro22= | |
| ENST00000379077.7:c.66T>C | ENSP00000368368.3:p.Pro22= | |
| ENST00000448076.7:c.66T>C | ENSP00000413452.3:p.Pro22= | |
| ENST00000452863.7:c.66T>C | ENSP00000415516.3:p.Pro22= | |
| NM_000378.4:c.66T>C | NP_000369.3:p.Pro22= | |
| NM_024424.3:c.66T>C | NP_077742.2:p.Pro22= | |
| NM_024426.4:c.66T>C | NP_077744.3:p.Pro22= | |
| NM_000378.5:c.81T>C | NP_000369.4:p.Pro27= | |
| NM_024424.4:c.81T>C | NP_077742.3:p.Pro27= | |
| NM_024426.5:c.81T>C | NP_077744.4:p.Pro27= | |
| NR_160306.1:n.260T>C | ||
| NM_000378.6:c.81T>C | NP_000369.4:p.Pro27= | |
| NM_024424.5:c.81T>C | NP_077742.3:p.Pro27= | |
| NM_024426.6:c.81T>C MANE Select | NP_077744.4:p.Pro27= |