Linked Data
dbSNP Id:
rs1436746563
gnomAD v4:
3-47000285-C-A
MyVariant Identifiers:
chr3:g.47041775C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.47000285C>A , CM000665.2:g.47000285C>A | GRCh38 |
| NC_000003.11:g.47041775C>A , CM000665.1:g.47041775C>A | GRCh37 |
| NC_000003.10:g.47016779C>A | NCBI36 |
| NG_031914.1:g.25603C>A , LRG_568:g.25603C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450053.8:c.4186C>A MANE Select | ENSP00000415034.2:p.Arg1396= | |
| ENST00000651747.1:c.4084C>A | ENSP00000499216.1:p.Arg1362= | |
| ENST00000416683.5:c.2049C>A | ||
| ENST00000450053.7:c.4186C>A | ENSP00000415034.2:p.Arg1396= | |
| NM_015175.2:c.4186C>A , LRG_568t1:c.4186C>A | NP_055990.1:p.Arg1396= | |
| XM_005264992.2:c.4084C>A | XP_005265049.1:p.Arg1362= | |
| XM_005264993.2:c.658C>A | XP_005265050.1:p.Arg220= | |
| XM_006713072.2:c.4105C>A | XP_006713135.1:p.Arg1369= | |
| XM_011533532.1:c.4165C>A | XP_011531834.1:p.Arg1389= | |
| XM_011533533.1:c.4186C>A | XP_011531835.1:p.Arg1396= | |
| XM_011533534.1:c.3817C>A | XP_011531836.1:p.Arg1273= | |
| XM_011533535.1:c.3646C>A | XP_011531837.1:p.Arg1216= | |
| XM_011533536.1:c.3532C>A | XP_011531838.1:p.Arg1178= | |
| XM_011533537.1:c.3094C>A | XP_011531839.1:p.Arg1032= | |
| XR_940397.1:n.4362C>A | ||
| XR_940398.1:n.4362C>A | ||
| NM_001365116.1:c.4084C>A | NP_001352045.1:p.Arg1362= | |
| XM_006713072.3:c.4105C>A | XP_006713135.1:p.Arg1369= | |
| XM_011533533.2:c.4186C>A | XP_011531835.1:p.Arg1396= | |
| XM_017006010.1:c.4186C>A | XP_016861499.1:p.Arg1396= | |
| XM_017006011.1:c.4165C>A | XP_016861500.1:p.Arg1389= | |
| XM_017006012.1:c.4105C>A | XP_016861501.1:p.Arg1369= | |
| XM_017006013.1:c.4186C>A | XP_016861502.1:p.Arg1396= | |
| XM_017006014.1:c.4084C>A | XP_016861503.1:p.Arg1362= | |
| XM_017006015.1:c.3817C>A | XP_016861504.1:p.Arg1273= | |
| XM_017006016.1:c.3646C>A | XP_016861505.1:p.Arg1216= | |
| XM_017006017.1:c.658C>A | XP_016861506.1:p.Arg220= | |
| XR_940397.2:n.4362C>A | ||
| NM_001365116.2:c.4084C>A | NP_001352045.1:p.Arg1362= | |
| NM_015175.3:c.4186C>A MANE Select | NP_055990.1:p.Arg1396= |