Linked Data
ClinVar Variation Id:
499039
dbSNP Id:
rs779268926
gnomAD v2:
2-179600302-G-T
gnomAD v4:
2-178735575-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178735575G>T , CM000664.2:g.178735575G>T | GRCh38 |
| NC_000002.11:g.179600302G>T , CM000664.1:g.179600302G>T | GRCh37 |
| NC_000002.10:g.179308547G>T | NCBI36 |
| NG_011618.3:g.100228C>A , LRG_391:g.100228C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.11139C>A | ENSP00000343764.6:p.Thr3713= | |
| ENST00000342175.11:c.13858+2507C>A | ENSP00000340554.6:n.13858+2507C>A | |
| ENST00000359218.10:c.13657+2507C>A | ENSP00000352154.5:n.13657+2507C>A | |
| ENST00000342175.10:c.13858+2507C>A | ENSP00000340554.6:n.13858+2507C>A | |
| ENST00000342992.10:c.11139C>A | ENSP00000343764.6:p.Thr3713= | |
| ENST00000359218.9:c.13657+2507C>A | ENSP00000352154.5:n.13657+2507C>A | |
| ENST00000460472.6:c.13282+2507C>A | ENSP00000434586.1:n.13282+2507C>A | |
| ENST00000589042.5:c.14871C>A MANE Select | ENSP00000467141.1:p.Thr4957= | |
| ENST00000591111.5:c.13920C>A | ENSP00000465570.1:p.Thr4640= | |
| ENST00000615779.4:c.13920C>A | ENSP00000483597.1:p.Thr4640= | |
| NM_001256850.1:c.13920C>A | NP_001243779.1:p.Thr4640= | |
| NM_001267550.2:c.14871C>A MANE Select | NP_001254479.2:p.Thr4957= | |
| NM_003319.4:c.13282+2507C>A | NP_003310.4:n.13282+2507C>A | |
| NM_133378.4:c.11139C>A | NP_596869.4:p.Thr3713= | |
| NM_133432.3:c.13657+2507C>A | NP_597676.3:n.13657+2507C>A | |
| NM_133437.4:c.13858+2507C>A | NP_597681.4:n.13858+2507C>A | |
| XM_011511729.1:c.13968C>A | XP_011510031.1:p.Thr4656= | |
| XM_011511730.1:c.13468+2507C>A | XP_011510032.1:n.13468+2507C>A | |
| XM_011511731.1:c.13327+2507C>A | XP_011510033.1:n.13327+2507C>A | |
| XM_017004819.1:c.13923C>A | XP_016860308.1:p.Thr4641= | |
| XM_017004820.1:c.11142C>A | XP_016860309.1:p.Thr3714= | |
| XM_017004821.1:c.11139C>A | XP_016860310.1:p.Thr3713= | |
| XM_017004822.1:c.13923C>A | XP_016860311.1:p.Thr4641= | |
| XM_017004823.1:c.13423+2507C>A | XP_016860312.1:n.13423+2507C>A | |
| XM_024453094.1:c.13923C>A | XP_024308862.1:p.Thr4641= | |
| XM_024453095.1:c.13923C>A | XP_024308863.1:p.Thr4641= | |
| XM_024453096.1:c.13923C>A | XP_024308864.1:p.Thr4641= | |
| XM_024453097.1:c.13923C>A | XP_024308865.1:p.Thr4641= | |
| XM_024453098.1:c.13923C>A | XP_024308866.1:p.Thr4641= | |
| XM_024453099.1:c.13423+2507C>A | XP_024308867.1:n.13423+2507C>A |