Linked Data
ClinVar Variation Id:
517478
dbSNP Id:
rs182626712
ExAC:
5:90040927 A / G
gnomAD v2:
5-90040927-A-G
gnomAD v3:
5-90745110-A-G
gnomAD v4:
5-90745110-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.90745110A>G , CM000667.2:g.90745110A>G | GRCh38 |
| NC_000005.9:g.90040927A>G , CM000667.1:g.90040927A>G | GRCh37 |
| NC_000005.8:g.90076683A>G | NCBI36 |
| NG_007083.1:g.191311A>G | |
| NG_007083.2:g.220767A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405460.9:c.10614A>G MANE Select | ENSP00000384582.2:p.Gln3538= | |
| ENST00000639431.1:c.265+68901A>G | ENSP00000491057.1:n.265+68901A>G | |
| ENST00000640374.1:n.3758A>G | ||
| ENST00000640464.1:n.1033A>G | ||
| ENST00000405460.6:c.10614A>G | ENSP00000384582.2:p.Gln3538= | |
| ENST00000509621.1:c.3311A>G | ||
| NM_032119.3:c.10614A>G | NP_115495.3:p.Gln3538= | |
| NR_003149.1:n.10627A>G | ||
| XM_011543675.1:c.10611A>G | XP_011541977.1:p.Gln3537= | |
| XM_011543676.1:c.10533A>G | XP_011541978.1:p.Gln3511= | |
| XM_011543677.1:c.7917A>G | XP_011541979.1:p.Gln2639= | |
| XM_011543678.1:c.10614A>G | XP_011541980.1:p.Gln3538= | |
| XM_011543679.1:c.10614A>G | XP_011541981.1:p.Gln3538= | |
| NM_032119.4:c.10614A>G MANE Select | NP_115495.3:p.Gln3538= | |
| XM_017009963.2:c.10635A>G | XP_016865452.1:p.Gln3545= | |
| XM_017009964.2:c.10632A>G | XP_016865453.1:p.Gln3544= | |
| XM_017009965.1:c.10632A>G | XP_016865454.1:p.Gln3544= | |
| XM_017009966.2:c.10554A>G | XP_016865455.1:p.Gln3518= | |
| XM_017009967.1:c.10539A>G | XP_016865456.1:p.Gln3513= | |
| XM_017009968.2:c.10635A>G | XP_016865457.1:p.Gln3545= | |
| XM_017009969.2:c.10635A>G | XP_016865458.1:p.Gln3545= | |
| XM_017009970.2:c.10635A>G | XP_016865459.1:p.Gln3545= | |
| XM_017009971.2:c.10635A>G | XP_016865460.1:p.Gln3545= | |
| XM_017009972.1:c.3753A>G | XP_016865461.1:p.Gln1251= | |
| XM_017009973.1:c.3732A>G | XP_016865462.1:p.Gln1244= | |
| XM_017009974.2:c.10635A>G | XP_016865463.1:p.Gln3545= | |
| NR_003149.2:n.10630A>G |