Linked Data
ClinVar Variation Id:
46645
ClinVar RCV Id:
RCV000039915
RCV000272168
RCV000329497
RCV000330701
RCV000253545
RCV000387580
RCV000462864
RCV000370173
RCV001311557
RCV001170639
dbSNP Id:
rs146219199
ExAC:
2:179594067 A / G
gnomAD v2:
2-179594067-A-G
gnomAD v3:
2-178729340-A-G
gnomAD v4:
2-178729340-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178729340A>G , CM000664.2:g.178729340A>G | GRCh38 |
| NC_000002.11:g.179594067A>G , CM000664.1:g.179594067A>G | GRCh37 |
| NC_000002.10:g.179302312A>G | NCBI36 |
| NG_011618.3:g.106463T>C , LRG_391:g.106463T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.15084T>C | ENSP00000343764.6:p.Ile5028= | |
| ENST00000342175.11:c.13858+8742T>C | ENSP00000340554.6:n.13858+8742T>C | |
| ENST00000359218.10:c.13657+8742T>C | ENSP00000352154.5:n.13657+8742T>C | |
| ENST00000342175.10:c.13858+8742T>C | ENSP00000340554.6:n.13858+8742T>C | |
| ENST00000342992.10:c.15084T>C | ENSP00000343764.6:p.Ile5028= | |
| ENST00000359218.9:c.13657+8742T>C | ENSP00000352154.5:n.13657+8742T>C | |
| ENST00000460472.6:c.13282+8742T>C | ENSP00000434586.1:n.13282+8742T>C | |
| ENST00000589042.5:c.18816T>C MANE Select | ENSP00000467141.1:p.Ile6272= | |
| ENST00000591111.5:c.17865T>C | ENSP00000465570.1:p.Ile5955= | |
| ENST00000615779.4:c.17865T>C | ENSP00000483597.1:p.Ile5955= | |
| NM_001256850.1:c.17865T>C | NP_001243779.1:p.Ile5955= | |
| NM_001267550.2:c.18816T>C MANE Select | NP_001254479.2:p.Ile6272= | |
| NM_003319.4:c.13282+8742T>C | NP_003310.4:n.13282+8742T>C | |
| NM_133378.4:c.15084T>C | NP_596869.4:p.Ile5028= | |
| NM_133432.3:c.13657+8742T>C | NP_597676.3:n.13657+8742T>C | |
| NM_133437.4:c.13858+8742T>C | NP_597681.4:n.13858+8742T>C | |
| XM_011511729.1:c.17913T>C | XP_011510031.1:p.Ile5971= | |
| XM_011511730.1:c.13468+8742T>C | XP_011510032.1:n.13468+8742T>C | |
| XM_011511731.1:c.13327+8742T>C | XP_011510033.1:n.13327+8742T>C | |
| XM_017004819.1:c.17868T>C | XP_016860308.1:p.Ile5956= | |
| XM_017004820.1:c.15087T>C | XP_016860309.1:p.Ile5029= | |
| XM_017004821.1:c.15084T>C | XP_016860310.1:p.Ile5028= | |
| XM_017004822.1:c.17868T>C | XP_016860311.1:p.Ile5956= | |
| XM_017004823.1:c.13423+8742T>C | XP_016860312.1:n.13423+8742T>C | |
| XM_024453094.1:c.17868T>C | XP_024308862.1:p.Ile5956= | |
| XM_024453095.1:c.17868T>C | XP_024308863.1:p.Ile5956= | |
| XM_024453096.1:c.17868T>C | XP_024308864.1:p.Ile5956= | |
| XM_024453097.1:c.17868T>C | XP_024308865.1:p.Ile5956= | |
| XM_024453098.1:c.17868T>C | XP_024308866.1:p.Ile5956= | |
| XM_024453099.1:c.13423+8742T>C | XP_024308867.1:n.13423+8742T>C |