Linked Data
ClinVar Variation Id:
391954
dbSNP Id:
rs184512279
ExAC:
5:147486659 G / A
gnomAD v2:
5-147486659-G-A
gnomAD v3:
5-148107096-G-A
gnomAD v4:
5-148107096-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148107096G>A , CM000667.2:g.148107096G>A | GRCh38 |
| NC_000005.9:g.147486659G>A , CM000667.1:g.147486659G>A | GRCh37 |
| NC_000005.8:g.147466852G>A | NCBI36 |
| NG_009633.1:g.48125G>A , LRG_110:g.48125G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000481286.6:n.1148G>A | ||
| ENST00000256084.8:c.1539G>A MANE Select | ENSP00000256084.7:p.Glu513= | |
| ENST00000256084.7:c.1539G>A | ENSP00000256084.7:p.Glu513= | |
| ENST00000359874.7:c.1539G>A | ENSP00000352936.3:p.Glu513= | |
| ENST00000398454.5:c.1539G>A | ENSP00000381472.1:p.Glu513= | |
| ENST00000507988.5:n.1703G>A | ||
| ENST00000508733.5:c.1482G>A | ENSP00000421519.1:p.Glu494= | |
| NM_001127698.1:c.1539G>A | NP_001121170.1:p.Glu513= | |
| NM_001127699.1:c.1539G>A | NP_001121171.1:p.Glu513= | |
| NM_006846.3:c.1539G>A , LRG_110t1:c.1539G>A | NP_006837.2:p.Glu513= | |
| XM_011537550.1:c.1482G>A | XP_011535852.1:p.Glu494= | |
| XM_011537551.1:c.1455G>A | XP_011535853.1:p.Glu485= | |
| XM_011537551.2:c.1455G>A | XP_011535853.1:p.Glu485= | |
| NM_001127698.2:c.1539G>A | NP_001121170.1:p.Glu513= | |
| NM_001127699.2:c.1539G>A | NP_001121171.1:p.Glu513= | |
| NM_006846.4:c.1539G>A MANE Select | NP_006837.2:p.Glu513= |