Linked Data
ClinVar Variation Id:
46699
ClinVar RCV Id:
RCV000039969
RCV001065236
RCV001130568
RCV001130567
RCV001130569
RCV001130565
RCV001130566
RCV001507605
RCV003149640
RCV004534869
dbSNP Id:
rs183482849
ExAC:
2:179587128 A / T
gnomAD v2:
2-179587128-A-T
gnomAD v3:
2-178722401-A-T
gnomAD v4:
2-178722401-A-T
PubMed:
PMID:24503780
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178722401A>T , CM000664.2:g.178722401A>T | GRCh38 |
| NC_000002.11:g.179587128A>T , CM000664.1:g.179587128A>T | GRCh37 |
| NC_000002.10:g.179295373A>T | NCBI36 |
| NG_011618.3:g.113402T>A , LRG_391:g.113402T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.18654T>A | ENSP00000343764.6:p.Asp6218Glu | |
| ENST00000342175.11:c.13858+15681T>A | ENSP00000340554.6:n.13858+15681T>A | |
| ENST00000359218.10:c.13657+15681T>A | ENSP00000352154.5:n.13657+15681T>A | |
| ENST00000342175.10:c.13858+15681T>A | ENSP00000340554.6:n.13858+15681T>A | |
| ENST00000342992.10:c.18654T>A | ENSP00000343764.6:p.Asp6218Glu | |
| ENST00000359218.9:c.13657+15681T>A | ENSP00000352154.5:n.13657+15681T>A | |
| ENST00000460472.6:c.13282+15681T>A | ENSP00000434586.1:n.13282+15681T>A | |
| ENST00000589042.5:c.22386T>A MANE Select | ENSP00000467141.1:p.Asp7462Glu | |
| ENST00000591111.5:c.21435T>A | ENSP00000465570.1:p.Asp7145Glu | |
| ENST00000615779.4:c.21435T>A | ENSP00000483597.1:p.Asp7145Glu | |
| NM_001256850.1:c.21435T>A | NP_001243779.1:p.Asp7145Glu | |
| NM_001267550.2:c.22386T>A MANE Select | NP_001254479.2:p.Asp7462Glu | |
| NM_003319.4:c.13282+15681T>A | NP_003310.4:n.13282+15681T>A | |
| NM_133378.4:c.18654T>A | NP_596869.4:p.Asp6218Glu | |
| NM_133432.3:c.13657+15681T>A | NP_597676.3:n.13657+15681T>A | |
| NM_133437.4:c.13858+15681T>A | NP_597681.4:n.13858+15681T>A | |
| XM_011511729.1:c.21483T>A | XP_011510031.1:p.Asp7161Glu | |
| XM_011511730.1:c.13468+15681T>A | XP_011510032.1:n.13468+15681T>A | |
| XM_011511731.1:c.13327+15681T>A | XP_011510033.1:n.13327+15681T>A | |
| XM_017004819.1:c.21438T>A | XP_016860308.1:p.Asp7146Glu | |
| XM_017004820.1:c.18657T>A | XP_016860309.1:p.Asp6219Glu | |
| XM_017004821.1:c.18654T>A | XP_016860310.1:p.Asp6218Glu | |
| XM_017004822.1:c.21438T>A | XP_016860311.1:p.Asp7146Glu | |
| XM_017004823.1:c.13423+15681T>A | XP_016860312.1:n.13423+15681T>A | |
| XM_024453094.1:c.21438T>A | XP_024308862.1:p.Asp7146Glu | |
| XM_024453095.1:c.21438T>A | XP_024308863.1:p.Asp7146Glu | |
| XM_024453096.1:c.21438T>A | XP_024308864.1:p.Asp7146Glu | |
| XM_024453097.1:c.21438T>A | XP_024308865.1:p.Asp7146Glu | |
| XM_024453098.1:c.21438T>A | XP_024308866.1:p.Asp7146Glu | |
| XM_024453099.1:c.13423+15681T>A | XP_024308867.1:n.13423+15681T>A |