Linked Data
ClinVar Variation Id:
463336
ClinVar RCV Id:
RCV000608084
RCV001144566
RCV001841472
RCV002330862
RCV003539915
RCV001144567
RCV001144568
RCV001144569
RCV001144570
RCV001144571
dbSNP Id:
rs199473246
ExAC:
3:38598725 C / T
gnomAD v2:
3-38598725-C-T
gnomAD v3:
3-38557234-C-T
gnomAD v4:
3-38557234-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.38557234C>T , CM000665.2:g.38557234C>T | GRCh38 |
| NC_000003.11:g.38598725C>T , CM000665.1:g.38598725C>T | GRCh37 |
| NC_000003.10:g.38573729C>T | NCBI36 |
| NG_008934.1:g.97439G>A , LRG_289:g.97439G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327956.7:c.4293G>A | ENSP00000333674.7:p.Arg1431= | |
| ENST00000333535.9:c.4296G>A | ENSP00000328968.4:p.Arg1432= | |
| ENST00000413689.6:c.4296G>A MANE Plus Clinical | ENSP00000410257.1:p.Arg1432= | |
| ENST00000423572.7:c.4293G>A MANE Select | ENSP00000398266.2:p.Arg1431= | |
| ENST00000333535.8:c.4296G>A | ENSP00000328968.4:p.Arg1432= | |
| ENST00000413689.5:c.4296G>A | ENSP00000410257.1:p.Arg1432= | |
| ENST00000414099.6:c.4246-656G>A | ENSP00000398962.2:n.4246-656G>A | |
| ENST00000423572.6:c.4293G>A | ENSP00000398266.2:p.Arg1431= | |
| ENST00000425664.5:c.4246-656G>A | ENSP00000416634.1:n.4246-656G>A | |
| ENST00000449557.6:c.4134G>A | ENSP00000413996.2:p.Arg1378= | |
| ENST00000450102.6:c.4134G>A | ENSP00000403355.2:p.Arg1378= | |
| ENST00000451551.6:c.4134G>A | ENSP00000388797.2:p.Arg1378= | |
| ENST00000455624.6:c.4293G>A | ENSP00000399524.2:p.Arg1431= | |
| NM_000335.4:c.4293G>A , LRG_289t2:c.4293G>A | NP_000326.2:p.Arg1431= | |
| NM_001099404.1:c.4296G>A , LRG_289t3:c.4296G>A | NP_001092874.1:p.Arg1432= | |
| NM_001099405.1:c.4246-656G>A | NP_001092875.1:n.4246-656G>A | |
| NM_001160160.1:c.4293G>A | NP_001153632.1:p.Arg1431= | |
| NM_001160161.1:c.4134G>A | NP_001153633.1:p.Arg1378= | |
| NM_198056.2:c.4296G>A , LRG_289t1:c.4296G>A | NP_932173.1:p.Arg1432= | |
| XM_006713282.2:c.4296G>A | XP_006713345.1:p.Arg1432= | |
| XM_011533991.1:c.4293G>A | XP_011532293.1:p.Arg1431= | |
| XM_011533992.1:c.4167G>A | XP_011532294.1:p.Arg1389= | |
| NM_001354701.1:c.4243-656G>A | NP_001341630.1:n.4243-656G>A | |
| XM_011533991.2:c.4293G>A | XP_011532293.1:p.Arg1431= | |
| XM_017007017.1:c.4134G>A | XP_016862506.1:p.Arg1378= | |
| NM_000335.5:c.4293G>A MANE Select | NP_000326.2:p.Arg1431= | |
| NM_001160160.2:c.4293G>A | NP_001153632.1:p.Arg1431= | |
| NM_001354701.2:c.4243-656G>A | NP_001341630.1:n.4243-656G>A | |
| NM_001099404.2:c.4296G>A MANE Plus Clinical | NP_001092874.1:p.Arg1432= | |
| NM_001099405.2:c.4246-656G>A | NP_001092875.1:n.4246-656G>A | |
| NM_001160161.2:c.4134G>A | NP_001153633.1:p.Arg1378= | |
| NM_198056.3:c.4296G>A | NP_932173.1:p.Arg1432= |