Linked Data
ClinVar Variation Id:
541145
dbSNP Id:
rs377567167
ExAC:
1:979373 G / A
gnomAD v2:
1-979373-G-A
gnomAD v3:
1-1043993-G-A
gnomAD v4:
1-1043993-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1043993G>A , CM000663.2:g.1043993G>A | GRCh38 |
| NC_000001.10:g.979373G>A , CM000663.1:g.979373G>A | GRCh37 |
| NC_000001.9:g.969236G>A | NCBI36 |
| NG_016346.1:g.28871G>A , LRG_198:g.28871G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379370.7:c.1969G>A MANE Select | ENSP00000368678.2:p.Glu657Lys | |
| ENST00000651234.1:c.1654G>A | ENSP00000499046.1:p.Glu552Lys | |
| ENST00000652369.1:c.1654G>A | ENSP00000498543.1:p.Glu552Lys | |
| ENST00000379370.6:c.1969G>A | ENSP00000368678.2:p.Glu657Lys | |
| ENST00000620552.4:c.1555G>A | ENSP00000484607.1:p.Glu519Lys | |
| NM_001305275.1:c.1969G>A | NP_001292204.1:p.Glu657Lys | |
| NM_198576.3:c.1969G>A | NP_940978.2:p.Glu657Lys | |
| XM_005244749.2:c.1969G>A | XP_005244806.1:p.Glu657Lys | |
| XM_006710635.2:c.1969G>A | XP_006710698.1:p.Glu657Lys | |
| XM_011541429.1:c.1969G>A | XP_011539731.1:p.Glu657Lys | |
| XM_011541430.1:c.1096G>A | XP_011539732.1:p.Glu366Lys | |
| XM_011541431.1:c.235G>A | XP_011539733.1:p.Glu79Lys | |
| XR_946650.1:n.2036G>A | ||
| NM_001364727.1:c.1654G>A | NP_001351656.1:p.Glu552Lys | |
| XM_005244749.3:c.1969G>A | XP_005244806.1:p.Glu657Lys | |
| XM_011541429.2:c.1969G>A | XP_011539731.1:p.Glu657Lys | |
| XR_946650.2:n.2040G>A | ||
| NM_001305275.2:c.1969G>A | NP_001292204.1:p.Glu657Lys | |
| NM_198576.4:c.1969G>A MANE Select | NP_940978.2:p.Glu657Lys | |
| NM_001364727.2:c.1654G>A | NP_001351656.1:p.Glu552Lys |