Linked Data
dbSNP Id:
rs762685794
ExAC:
3:47041856 A / G
gnomAD v2:
3-47041856-A-G
gnomAD v4:
3-47000366-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.47000366A>G , CM000665.2:g.47000366A>G | GRCh38 |
| NC_000003.11:g.47041856A>G , CM000665.1:g.47041856A>G | GRCh37 |
| NC_000003.10:g.47016860A>G | NCBI36 |
| NG_031914.1:g.25684A>G , LRG_568:g.25684A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450053.8:c.4267A>G MANE Select | ENSP00000415034.2:p.Ile1423Val | |
| ENST00000651747.1:c.4165A>G | ENSP00000499216.1:p.Ile1389Val | |
| ENST00000416683.5:c.2130A>G | ||
| ENST00000450053.7:c.4267A>G | ENSP00000415034.2:p.Ile1423Val | |
| NM_015175.2:c.4267A>G , LRG_568t1:c.4267A>G | NP_055990.1:p.Ile1423Val | |
| XM_005264992.2:c.4165A>G | XP_005265049.1:p.Ile1389Val | |
| XM_005264993.2:c.739A>G | XP_005265050.1:p.Ile247Val | |
| XM_006713072.2:c.4186A>G | XP_006713135.1:p.Ile1396Val | |
| XM_011533532.1:c.4246A>G | XP_011531834.1:p.Ile1416Val | |
| XM_011533533.1:c.4267A>G | XP_011531835.1:p.Ile1423Val | |
| XM_011533534.1:c.3898A>G | XP_011531836.1:p.Ile1300Val | |
| XM_011533535.1:c.3727A>G | XP_011531837.1:p.Ile1243Val | |
| XM_011533536.1:c.3613A>G | XP_011531838.1:p.Ile1205Val | |
| XM_011533537.1:c.3175A>G | XP_011531839.1:p.Ile1059Val | |
| XR_940397.1:n.4443A>G | ||
| XR_940398.1:n.4443A>G | ||
| NM_001365116.1:c.4165A>G | NP_001352045.1:p.Ile1389Val | |
| XM_006713072.3:c.4186A>G | XP_006713135.1:p.Ile1396Val | |
| XM_011533533.2:c.4267A>G | XP_011531835.1:p.Ile1423Val | |
| XM_017006010.1:c.4267A>G | XP_016861499.1:p.Ile1423Val | |
| XM_017006011.1:c.4246A>G | XP_016861500.1:p.Ile1416Val | |
| XM_017006012.1:c.4186A>G | XP_016861501.1:p.Ile1396Val | |
| XM_017006013.1:c.4267A>G | XP_016861502.1:p.Ile1423Val | |
| XM_017006014.1:c.4165A>G | XP_016861503.1:p.Ile1389Val | |
| XM_017006015.1:c.3898A>G | XP_016861504.1:p.Ile1300Val | |
| XM_017006016.1:c.3727A>G | XP_016861505.1:p.Ile1243Val | |
| XM_017006017.1:c.739A>G | XP_016861506.1:p.Ile247Val | |
| XR_940397.2:n.4443A>G | ||
| NM_001365116.2:c.4165A>G | NP_001352045.1:p.Ile1389Val | |
| NM_015175.3:c.4267A>G MANE Select | NP_055990.1:p.Ile1423Val |