Linked Data
ClinVar Variation Id:
2354925
ClinVar RCV Id:
RCV004197428
dbSNP Id:
rs374767571
gnomAD v3:
8-134602329-G-C
gnomAD v4:
8-134602329-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.134602329G>C , CM000670.2:g.134602329G>C | GRCh38 |
| NC_000008.10:g.135614572G>C , CM000670.1:g.135614572G>C | GRCh37 |
| NC_000008.9:g.135683754G>C | NCBI36 |
| NG_016356.1:g.115721C>G | |
| NG_016356.2:g.115721C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377838.8:c.1390C>G MANE Select | ENSP00000367069.3:p.Arg464Gly | |
| ENST00000377838.7:c.1390C>G | ENSP00000367069.3:p.Arg464Gly | |
| ENST00000429442.6:c.1354C>G | ENSP00000394501.2:p.Arg452Gly | |
| ENST00000520214.5:c.1354C>G | ENSP00000428483.1:p.Arg452Gly | |
| ENST00000520356.5:c.1354C>G | ENSP00000427879.1:p.Arg452Gly | |
| ENST00000520727.5:c.1354C>G | ENSP00000427831.1:p.Arg452Gly | |
| ENST00000522974.5:n.1495C>G | ||
| ENST00000523243.5:c.1390C>G | ENSP00000429930.1:p.Arg464Gly | |
| ENST00000523399.5:c.1204C>G | ENSP00000429091.1:p.Arg402Gly | |
| ENST00000523924.5:c.*1372C>G | ENSP00000429050.1:n.*1372C>G | |
| NM_001029939.3:c.1354C>G | NP_001025110.2:p.Arg452Gly | |
| NM_001167583.2:c.1354C>G | NP_001161055.1:p.Arg452Gly | |
| NM_001174157.1:c.1204C>G | NP_001167628.1:p.Arg402Gly | |
| NM_001174158.1:c.1354C>G | NP_001167629.1:p.Arg452Gly | |
| NM_001289394.1:c.1354C>G | NP_001276323.1:p.Arg452Gly | |
| NM_020863.3:c.1390C>G | NP_065914.2:p.Arg464Gly | |
| NR_110323.1:n.1576C>G | ||
| XM_011517203.1:c.1354C>G | XP_011515505.1:p.Arg452Gly | |
| XM_011517204.1:c.1204C>G | XP_011515506.1:p.Arg402Gly | |
| XM_011517205.1:c.1354C>G | XP_011515507.1:p.Arg452Gly | |
| XM_011517206.1:c.1354C>G | XP_011515508.1:p.Arg452Gly | |
| XR_928343.1:n.1371C>G | ||
| XM_011517204.2:c.1204C>G | XP_011515506.1:p.Arg402Gly | |
| XM_011517206.2:c.1354C>G | XP_011515508.1:p.Arg452Gly | |
| XM_017013716.1:c.1354C>G | XP_016869205.1:p.Arg452Gly | |
| XR_001745568.1:n.1371C>G | ||
| XR_001745569.1:n.1371C>G | ||
| XR_001745570.1:n.1371C>G | ||
| XR_928343.2:n.1371C>G | ||
| NM_020863.4:c.1390C>G MANE Select | NP_065914.2:p.Arg464Gly | |
| NM_001029939.4:c.1354C>G | NP_001025110.2:p.Arg452Gly | |
| NM_001167583.3:c.1354C>G | NP_001161055.1:p.Arg452Gly | |
| NM_001174157.2:c.1204C>G | NP_001167628.1:p.Arg402Gly | |
| NM_001174158.2:c.1354C>G | NP_001167629.1:p.Arg452Gly | |
| NM_001289394.2:c.1354C>G | NP_001276323.1:p.Arg452Gly | |
| NR_110323.2:n.1558C>G |