Linked Data
ClinVar Variation Id:
1594990
ClinVar RCV Id:
RCV002108239
dbSNP Id:
rs2124537148
MyVariant Identifiers:
chr2:g.39250060A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.39022919A>G , CM000664.2:g.39022919A>G | GRCh38 |
| NC_000002.11:g.39250060A>G , CM000664.1:g.39250060A>G | GRCh37 |
| NC_000002.10:g.39103564A>G | NCBI36 |
| NG_007530.1:g.102545T>C , LRG_754:g.102545T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000472480.2:n.1389T>C | ||
| ENST00000685279.1:c.276T>C | ENSP00000509424.1:p.Asp92= | |
| ENST00000688043.1:n.1730T>C | ||
| ENST00000689668.1:n.1516T>C | ||
| ENST00000690876.1:c.1398T>C | ENSP00000508955.1:p.Asp466= | |
| ENST00000691229.1:c.1398T>C | ENSP00000510437.1:p.Asp466= | |
| ENST00000692089.1:c.1398T>C | ENSP00000508626.1:p.Asp466= | |
| ENST00000692620.1:c.276T>C | ENSP00000509311.1:p.Asp92= | |
| ENST00000402219.8:c.1509T>C MANE Select | ENSP00000384675.2:p.Asp503= | |
| ENST00000395038.6:c.1509T>C | ENSP00000378479.2:p.Asp503= | |
| ENST00000402219.6:c.1509T>C | ENSP00000384675.2:p.Asp503= | |
| ENST00000426016.5:c.1509T>C | ENSP00000387784.1:p.Asp503= | |
| ENST00000472480.1:n.353T>C | ||
| NM_005633.3:c.1509T>C , LRG_754t1:c.1509T>C | NP_005624.2:p.Asp503= | |
| XM_005264515.3:c.1509T>C | XP_005264572.1:p.Asp503= | |
| XM_011533060.1:c.1602T>C | XP_011531362.1:p.Asp534= | |
| XM_011533061.1:c.1602T>C | XP_011531363.1:p.Asp534= | |
| XM_011533062.1:c.1488T>C | XP_011531364.1:p.Asp496= | |
| XM_011533063.1:c.1485T>C | XP_011531365.1:p.Asp495= | |
| XM_011533064.1:c.1338T>C | XP_011531366.1:p.Asp446= | |
| XM_011533065.1:c.1602T>C | XP_011531367.1:p.Asp534= | |
| XM_011533066.1:c.444T>C | XP_011531368.1:p.Asp148= | |
| XM_005264515.4:c.1509T>C | XP_005264572.1:p.Asp503= | |
| XM_011533062.2:c.1488T>C | XP_011531364.1:p.Asp496= | |
| XM_011533064.2:c.1338T>C | XP_011531366.1:p.Asp446= | |
| NM_001382394.1:c.1488T>C | NP_001369323.1:p.Asp496= | |
| NM_001382395.1:c.1509T>C | NP_001369324.1:p.Asp503= | |
| NM_005633.4:c.1509T>C MANE Select | NP_005624.2:p.Asp503= |