Linked Data
dbSNP Id:
rs774937754
ExAC:
8:100887858 G / C
gnomAD v2:
8-100887858-G-C
gnomAD v4:
8-99875630-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99875630G>C , CM000670.2:g.99875630G>C | GRCh38 |
| NC_000008.10:g.100887858G>C , CM000670.1:g.100887858G>C | GRCh37 |
| NC_000008.9:g.100957034G>C | NCBI36 |
| NG_007098.2:g.867365G>C , LRG_351:g.867365G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682153.1:c.*1687G>C (VPS13B) | ENSP00000507923.1:n.*1687G>C | |
| ENST00000682358.1:n.12663G>C (VPS13B) | ||
| ENST00000683334.1:c.*7715G>C (VPS13B) | ENSP00000507369.1:n.*7715G>C | |
| ENST00000357162.7:c.11958G>C (VPS13B) MANE Select | ENSP00000349685.2:p.Met3986Ile | |
| ENST00000358544.7:c.12033G>C (VPS13B) MANE Plus Clinical | ENSP00000351346.2:p.Met4011Ile | |
| ENST00000357162.6:c.11958G>C (VPS13B) | ENSP00000349685.2:p.Met3986Ile | |
| ENST00000358544.6:c.12033G>C (VPS13B) | ENSP00000351346.2:p.Met4011Ile | |
| ENST00000493587.1:n.1535G>C (VPS13B) | ||
| ENST00000520517.5:c.*142-538C>G (COX6C) | ENSP00000429991.1:n.*142-538C>G | |
| ENST00000522934.5:c.*142-2337C>G (COX6C) | ENSP00000428702.1:n.*142-2337C>G | |
| NM_017890.4:c.12033G>C , LRG_351t1:c.12033G>C (VPS13B) | NP_060360.3:p.Met4011Ile | |
| NM_152564.4:c.11958G>C , LRG_351t2:c.11958G>C (VPS13B) | NP_689777.3:p.Met3986Ile | |
| XM_005250800.2:c.12033G>C (VPS13B) | XP_005250857.1:p.Met4011Ile | |
| XM_005250801.3:c.12033G>C (VPS13B) | XP_005250858.1:p.Met4011Ile | |
| XM_011516848.1:c.12030G>C (VPS13B) | XP_011515150.1:p.Met4010Ile | |
| XM_011516849.1:c.11955G>C (VPS13B) | XP_011515151.1:p.Met3985Ile | |
| XM_011516850.1:c.11655G>C (VPS13B) | XP_011515152.1:p.Met3885Ile | |
| XM_011516851.1:c.8919G>C (VPS13B) | XP_011515153.1:p.Met2973Ile | |
| XM_011516852.1:c.8919G>C (VPS13B) | XP_011515154.1:p.Met2973Ile | |
| XM_011516854.1:c.7812G>C (VPS13B) | XP_011515156.1:p.Met2604Ile | |
| XM_005250800.3:c.12033G>C (VPS13B) | XP_005250857.1:p.Met4011Ile | |
| XM_005250801.5:c.12033G>C (VPS13B) | XP_005250858.1:p.Met4011Ile | |
| XM_011516848.2:c.12030G>C (VPS13B) | XP_011515150.1:p.Met4010Ile | |
| XM_011516849.2:c.11955G>C (VPS13B) | XP_011515151.1:p.Met3985Ile | |
| XM_011516850.2:c.11655G>C (VPS13B) | XP_011515152.1:p.Met3885Ile | |
| XM_011516851.2:c.8919G>C (VPS13B) | XP_011515153.1:p.Met2973Ile | |
| XM_011516852.2:c.8919G>C (VPS13B) | XP_011515154.1:p.Met2973Ile | |
| XM_011516854.2:c.7812G>C (VPS13B) | XP_011515156.1:p.Met2604Ile | |
| XM_017013109.1:c.11838G>C (VPS13B) | XP_016868598.1:p.Met3946Ile | |
| XM_017013111.1:c.8919G>C (VPS13B) | XP_016868600.1:p.Met2973Ile | |
| XM_017013112.1:c.7590G>C (VPS13B) | XP_016868601.1:p.Met2530Ile | |
| XM_024447074.1:c.10818G>C (VPS13B) | XP_024302842.1:p.Met3606Ile | |
| NM_017890.5:c.12033G>C (VPS13B) MANE Plus Clinical | NP_060360.3:p.Met4011Ile | |
| NM_152564.5:c.11958G>C (VPS13B) MANE Select | NP_689777.3:p.Met3986Ile |