Linked Data
ClinVar Variation Id:
3046982
ClinVar RCV Id:
RCV003934631
dbSNP Id:
rs199842407
ExAC:
3:47041777 G / A
gnomAD v2:
3-47041777-G-A
gnomAD v3:
3-47000287-G-A
gnomAD v4:
3-47000287-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.47000287G>A , CM000665.2:g.47000287G>A | GRCh38 |
| NC_000003.11:g.47041777G>A , CM000665.1:g.47041777G>A | GRCh37 |
| NC_000003.10:g.47016781G>A | NCBI36 |
| NG_031914.1:g.25605G>A , LRG_568:g.25605G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450053.8:c.4188G>A MANE Select | ENSP00000415034.2:p.Arg1396= | |
| ENST00000651747.1:c.4086G>A | ENSP00000499216.1:p.Arg1362= | |
| ENST00000416683.5:c.2051G>A | ||
| ENST00000450053.7:c.4188G>A | ENSP00000415034.2:p.Arg1396= | |
| NM_015175.2:c.4188G>A , LRG_568t1:c.4188G>A | NP_055990.1:p.Arg1396= | |
| XM_005264992.2:c.4086G>A | XP_005265049.1:p.Arg1362= | |
| XM_005264993.2:c.660G>A | XP_005265050.1:p.Arg220= | |
| XM_006713072.2:c.4107G>A | XP_006713135.1:p.Arg1369= | |
| XM_011533532.1:c.4167G>A | XP_011531834.1:p.Arg1389= | |
| XM_011533533.1:c.4188G>A | XP_011531835.1:p.Arg1396= | |
| XM_011533534.1:c.3819G>A | XP_011531836.1:p.Arg1273= | |
| XM_011533535.1:c.3648G>A | XP_011531837.1:p.Arg1216= | |
| XM_011533536.1:c.3534G>A | XP_011531838.1:p.Arg1178= | |
| XM_011533537.1:c.3096G>A | XP_011531839.1:p.Arg1032= | |
| XR_940397.1:n.4364G>A | ||
| XR_940398.1:n.4364G>A | ||
| NM_001365116.1:c.4086G>A | NP_001352045.1:p.Arg1362= | |
| XM_006713072.3:c.4107G>A | XP_006713135.1:p.Arg1369= | |
| XM_011533533.2:c.4188G>A | XP_011531835.1:p.Arg1396= | |
| XM_017006010.1:c.4188G>A | XP_016861499.1:p.Arg1396= | |
| XM_017006011.1:c.4167G>A | XP_016861500.1:p.Arg1389= | |
| XM_017006012.1:c.4107G>A | XP_016861501.1:p.Arg1369= | |
| XM_017006013.1:c.4188G>A | XP_016861502.1:p.Arg1396= | |
| XM_017006014.1:c.4086G>A | XP_016861503.1:p.Arg1362= | |
| XM_017006015.1:c.3819G>A | XP_016861504.1:p.Arg1273= | |
| XM_017006016.1:c.3648G>A | XP_016861505.1:p.Arg1216= | |
| XM_017006017.1:c.660G>A | XP_016861506.1:p.Arg220= | |
| XR_940397.2:n.4364G>A | ||
| NM_001365116.2:c.4086G>A | NP_001352045.1:p.Arg1362= | |
| NM_015175.3:c.4188G>A MANE Select | NP_055990.1:p.Arg1396= |