Linked Data
dbSNP Id:
rs889453633
gnomAD v2:
8-142178428-G-A
gnomAD v3:
8-141168329-G-A
gnomAD v4:
8-141168329-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.141168329G>A , CM000670.2:g.141168329G>A | GRCh38 |
| NC_000008.10:g.142178428G>A , CM000670.1:g.142178428G>A | GRCh37 |
| NC_000008.9:g.142247610G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000519811.6:c.2079G>A MANE Select | ENSP00000428714.1:p.Gln693= | |
| ENST00000262585.6:c.1839G>A | ENSP00000262585.2:p.Gln613= | |
| ENST00000424248.2:c.1683G>A | ENSP00000410594.1:p.Gln561= | |
| ENST00000518668.5:c.1852G>A | ||
| ENST00000519811.5:c.2079G>A | ENSP00000428714.1:p.Gln693= | |
| ENST00000520482.1:n.1620G>A | ||
| NM_014957.2:c.1839G>A | NP_055772.2:p.Gln613= | |
| XM_005250838.3:c.1878G>A | XP_005250895.2:p.Gln626= | |
| XM_005250839.2:c.1878G>A | XP_005250896.2:p.Gln626= | |
| XM_005250840.3:c.1722G>A | XP_005250897.2:p.Gln574= | |
| XM_005250841.2:c.1722G>A | XP_005250898.2:p.Gln574= | |
| XM_005250842.3:c.1845G>A | XP_005250899.1:p.Gln615= | |
| XM_005250843.3:c.1335G>A | XP_005250900.1:p.Gln445= | |
| XM_011516933.1:c.1878G>A | XP_011515235.1:p.Gln626= | |
| XM_011516934.1:c.1878G>A | XP_011515236.1:p.Gln626= | |
| XM_011516935.1:c.1512G>A | XP_011515237.1:p.Gln504= | |
| XM_011516936.1:c.1506G>A | XP_011515238.1:p.Gln502= | |
| XM_011516937.1:c.1878G>A | XP_011515239.1:p.Gln626= | |
| XM_011516938.1:c.1047G>A | XP_011515240.1:p.Gln349= | |
| XM_011516939.1:c.576G>A | XP_011515241.1:p.Gln192= | |
| XM_011516940.1:c.576G>A | XP_011515242.1:p.Gln192= | |
| XM_011516941.1:c.1878G>A | XP_011515243.1:p.Gln626= | |
| XM_011516942.1:c.1878G>A | XP_011515244.1:p.Gln626= | |
| XR_242384.2:n.2008G>A | ||
| XR_928310.1:n.2008G>A | ||
| XR_928311.1:n.2008G>A | ||
| XR_928312.1:n.2008G>A | ||
| NM_001352890.2:c.2079G>A | NP_001339819.2:p.Gln693= | |
| NM_001362798.1:c.2079G>A | NP_001349727.1:p.Gln693= | |
| NM_014957.4:c.1878G>A | NP_055772.3:p.Gln626= | |
| NR_148197.2:n.2175G>A | ||
| XM_005250840.5:c.1923G>A | XP_005250897.3:p.Gln641= | |
| XM_005250841.4:c.1923G>A | XP_005250898.3:p.Gln641= | |
| XM_005250842.4:c.1845G>A | XP_005250899.1:p.Gln615= | |
| XM_011516933.2:c.2079G>A | XP_011515235.2:p.Gln693= | |
| XM_011516934.3:c.2079G>A | XP_011515236.2:p.Gln693= | |
| XM_011516937.2:c.2079G>A | XP_011515239.2:p.Gln693= | |
| XM_011516938.3:c.1047G>A | XP_011515240.1:p.Gln349= | |
| XM_011516939.3:c.576G>A | XP_011515241.1:p.Gln192= | |
| XM_011516940.2:c.576G>A | XP_011515242.1:p.Gln192= | |
| XM_011516941.3:c.2079G>A | XP_011515243.2:p.Gln693= | |
| XM_017013241.1:c.1878G>A | XP_016868730.1:p.Gln626= | |
| XM_017013242.1:c.1335G>A | XP_016868731.1:p.Gln445= | |
| XM_017013243.1:c.615G>A | XP_016868732.1:p.Gln205= | |
| XR_001745497.2:n.2225G>A | ||
| XR_001745498.2:n.2225G>A | ||
| XR_928310.3:n.2225G>A | ||
| XR_928312.3:n.2225G>A | ||
| NM_001352890.3:c.2079G>A MANE Select | NP_001339819.2:p.Gln693= | |
| NM_001362798.2:c.2079G>A | NP_001349727.1:p.Gln693= | |
| NM_014957.5:c.1878G>A | NP_055772.3:p.Gln626= | |
| NR_148197.3:n.2198G>A |