Linked Data
dbSNP Id:
rs767755375
ExAC:
3:133494362 G / A
gnomAD v2:
3-133494362-G-A
gnomAD v3:
3-133775518-G-A
gnomAD v4:
3-133775518-G-A
COSMIC:
COSM3587667
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.133775518G>A , CM000665.2:g.133775518G>A | GRCh38 |
| NC_000003.11:g.133494362G>A , CM000665.1:g.133494362G>A | GRCh37 |
| NC_000003.10:g.134977052G>A | NCBI36 |
| NG_013080.1:g.34386G>A | |
| NG_013080.2:g.118521G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000402696.9:c.1773G>A MANE Select | ENSP00000385834.3:p.Glu591= | |
| ENST00000402696.7:c.1773G>A | ENSP00000385834.3:p.Glu591= | |
| ENST00000461695.1:c.504G>A | ||
| ENST00000467842.1:n.2767G>A | ||
| NM_001063.3:c.1773G>A | NP_001054.1:p.Glu591= | |
| XM_011513100.1:c.1773G>A | XP_011511402.1:p.Glu591= | |
| NM_001354703.1:c.1641G>A | NP_001341632.1:p.Glu547= | |
| NM_001354704.1:c.1392G>A | NP_001341633.1:p.Glu464= | |
| NM_001063.4:c.1773G>A MANE Select | NP_001054.2:p.Glu591= | |
| NM_001354703.2:c.1641G>A | NP_001341632.2:p.Glu547= | |
| NM_001354704.2:c.1392G>A | NP_001341633.2:p.Glu464= |