Linked Data
ClinVar Variation Id:
191992
ClinVar RCV Id:
RCV000172361
RCV000248449
RCV000340184
RCV000282781
RCV000371985
RCV000337132
RCV000394687
RCV000603350
RCV000770054
RCV001084484
dbSNP Id:
rs532102837
ExAC:
2:179542423 G / T
gnomAD v2:
2-179542423-G-T
gnomAD v3:
2-178677696-G-T
gnomAD v4:
2-178677696-G-T
MyVariant Identifiers:
chr2:g.179542423G>T (hg19)
chr2:g.179542423_179542435delinsTTACATATTCTTC (hg19)
chr2:g.178677696G>T (hg38)
chr2:g.178677696_178677708delinsTTACATATTCTTC (hg38)
PubMed:
PMID:23861362
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178677696G>T , CM000664.2:g.178677696G>T | GRCh38 |
| NC_000002.11:g.179542423G>T , CM000664.1:g.179542423G>T | GRCh37 |
| NC_000002.10:g.179250668G>T | NCBI36 |
| NG_011618.3:g.158107C>A , LRG_391:g.158107C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.30484C>A | ENSP00000343764.6:p.Pro10162Thr | |
| ENST00000342175.11:c.13859-35379C>A | ENSP00000340554.6:n.13859-35379C>A | |
| ENST00000359218.10:c.13658-35379C>A | ENSP00000352154.5:n.13658-35379C>A | |
| ENST00000342175.10:c.13859-35379C>A | ENSP00000340554.6:n.13859-35379C>A | |
| ENST00000342992.10:c.30484C>A | ENSP00000343764.6:p.Pro10162Thr | |
| ENST00000359218.9:c.13658-35379C>A | ENSP00000352154.5:n.13658-35379C>A | |
| ENST00000414766.5:c.2266+429C>A | ENSP00000401501.1:n.2266+429C>A | |
| ENST00000460472.6:c.13283-35379C>A | ENSP00000434586.1:n.13283-35379C>A | |
| ENST00000589042.5:c.34216C>A MANE Select | ENSP00000467141.1:p.Pro11406Thr | |
| ENST00000591111.5:c.33265C>A | ENSP00000465570.1:p.Pro11089Thr | |
| ENST00000615779.4:c.33265C>A | ENSP00000483597.1:p.Pro11089Thr | |
| NM_001256850.1:c.33265C>A | NP_001243779.1:p.Pro11089Thr | |
| NM_001267550.2:c.34216C>A MANE Select | NP_001254479.2:p.Pro11406Thr | |
| NM_003319.4:c.13283-35379C>A | NP_003310.4:n.13283-35379C>A | |
| NM_133378.4:c.30484C>A | NP_596869.4:p.Pro10162Thr | |
| NM_133432.3:c.13658-35379C>A | NP_597676.3:n.13658-35379C>A | |
| NM_133437.4:c.13859-35379C>A | NP_597681.4:n.13859-35379C>A | |
| XM_011511729.1:c.33313C>A | XP_011510031.1:p.Pro11105Thr | |
| XM_011511730.1:c.13469-35379C>A | XP_011510032.1:n.13469-35379C>A | |
| XM_011511731.1:c.13328-35379C>A | XP_011510033.1:n.13328-35379C>A | |
| XM_017004819.1:c.33268C>A | XP_016860308.1:p.Pro11090Thr | |
| XM_017004820.1:c.30487C>A | XP_016860309.1:p.Pro10163Thr | |
| XM_017004821.1:c.30484C>A | XP_016860310.1:p.Pro10162Thr | |
| XM_017004822.1:c.31684+429C>A | XP_016860311.1:n.31684+429C>A | |
| XM_017004823.1:c.13424-35379C>A | XP_016860312.1:n.13424-35379C>A | |
| XM_024453094.1:c.33046+429C>A | XP_024308862.1:n.33046+429C>A | |
| XM_024453095.1:c.33046+429C>A | XP_024308863.1:n.33046+429C>A | |
| XM_024453096.1:c.32476+429C>A | XP_024308864.1:n.32476+429C>A | |
| XM_024453097.1:c.31516+429C>A | XP_024308865.1:n.31516+429C>A | |
| XM_024453098.1:c.31435+429C>A | XP_024308866.1:n.31435+429C>A | |
| XM_024453099.1:c.13424-35379C>A | XP_024308867.1:n.13424-35379C>A |