Linked Data
ClinVar Variation Id:
46841
ClinVar RCV Id:
RCV000040111
RCV000172682
RCV000577956
RCV000578036
RCV000578117
RCV001129423
RCV000852879
RCV001084360
RCV001129424
RCV004541143
dbSNP Id:
rs111671438
ExAC:
2:179563606 C / A
gnomAD v2:
2-179563606-C-A
gnomAD v3:
2-178698879-C-A
gnomAD v4:
2-178698879-C-A
MyVariant Identifiers:
chr2:g.179563606C>A (hg19)
chr2:g.179563606_179563607delinsAT (hg19)
chr2:g.178698879C>A (hg38)
chr2:g.178698879_178698880delinsAT (hg38)
PubMed:
PMID:23861362
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178698879C>A , CM000664.2:g.178698879C>A | GRCh38 |
| NC_000002.11:g.179563606C>A , CM000664.1:g.179563606C>A | GRCh37 |
| NC_000002.10:g.179271851C>A | NCBI36 |
| NG_011618.3:g.136924G>T , LRG_391:g.136924G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.26986G>T | ENSP00000343764.6:p.Val8996Phe | |
| ENST00000342175.11:c.13858+39203G>T | ENSP00000340554.6:n.13858+39203G>T | |
| ENST00000359218.10:c.13657+39203G>T | ENSP00000352154.5:n.13657+39203G>T | |
| ENST00000342175.10:c.13858+39203G>T | ENSP00000340554.6:n.13858+39203G>T | |
| ENST00000342992.10:c.26986G>T | ENSP00000343764.6:p.Val8996Phe | |
| ENST00000359218.9:c.13657+39203G>T | ENSP00000352154.5:n.13657+39203G>T | |
| ENST00000414766.5:c.352G>T | ENSP00000401501.1:p.Val118Phe | |
| ENST00000460472.6:c.13282+39203G>T | ENSP00000434586.1:n.13282+39203G>T | |
| ENST00000589042.5:c.30718G>T MANE Select | ENSP00000467141.1:p.Val10240Phe | |
| ENST00000591111.5:c.29767G>T | ENSP00000465570.1:p.Val9923Phe | |
| ENST00000615779.4:c.29767G>T | ENSP00000483597.1:p.Val9923Phe | |
| NM_001256850.1:c.29767G>T | NP_001243779.1:p.Val9923Phe | |
| NM_001267550.2:c.30718G>T MANE Select | NP_001254479.2:p.Val10240Phe | |
| NM_003319.4:c.13282+39203G>T | NP_003310.4:n.13282+39203G>T | |
| NM_133378.4:c.26986G>T | NP_596869.4:p.Val8996Phe | |
| NM_133432.3:c.13657+39203G>T | NP_597676.3:n.13657+39203G>T | |
| NM_133437.4:c.13858+39203G>T | NP_597681.4:n.13858+39203G>T | |
| XM_011511729.1:c.29815G>T | XP_011510031.1:p.Val9939Phe | |
| XM_011511730.1:c.13468+39203G>T | XP_011510032.1:n.13468+39203G>T | |
| XM_011511731.1:c.13327+39203G>T | XP_011510033.1:n.13327+39203G>T | |
| XM_017004819.1:c.29770G>T | XP_016860308.1:p.Val9924Phe | |
| XM_017004820.1:c.26989G>T | XP_016860309.1:p.Val8997Phe | |
| XM_017004821.1:c.26986G>T | XP_016860310.1:p.Val8996Phe | |
| XM_017004822.1:c.29770G>T | XP_016860311.1:p.Val9924Phe | |
| XM_017004823.1:c.13423+39203G>T | XP_016860312.1:n.13423+39203G>T | |
| XM_024453094.1:c.29770G>T | XP_024308862.1:p.Val9924Phe | |
| XM_024453095.1:c.29770G>T | XP_024308863.1:p.Val9924Phe | |
| XM_024453096.1:c.29770G>T | XP_024308864.1:p.Val9924Phe | |
| XM_024453097.1:c.29770G>T | XP_024308865.1:p.Val9924Phe | |
| XM_024453098.1:c.29770G>T | XP_024308866.1:p.Val9924Phe | |
| XM_024453099.1:c.13423+39203G>T | XP_024308867.1:n.13423+39203G>T |