Linked Data
ClinVar Variation Id:
386884
dbSNP Id:
rs139861201
ExAC:
7:99704100 G / A
gnomAD v2:
7-99704100-G-A
gnomAD v3:
7-100106477-G-A
gnomAD v4:
7-100106477-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100106477G>A , CM000669.2:g.100106477G>A | GRCh38 |
| NC_000007.13:g.99704100G>A , CM000669.1:g.99704100G>A | GRCh37 |
| NC_000007.12:g.99542036G>A | NCBI36 |
| NG_016312.1:g.9971G>A | |
| NG_029454.1:g.18382C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000445295.2:c.1100G>A | ENSP00000393723.2:p.Arg367Gln | |
| ENST00000495154.2:n.1359G>A | ||
| ENST00000713591.1:c.1100G>A | ENSP00000518888.1:p.Arg367Gln | |
| ENST00000359593.9:c.1100G>A MANE Select | ENSP00000352603.4:p.Arg367Gln | |
| ENST00000359593.8:c.1100G>A | ENSP00000352603.4:p.Arg367Gln | |
| ENST00000416938.5:c.989G>A | ||
| ENST00000421755.5:c.1100G>A | ENSP00000412185.1:p.Arg367Gln | |
| ENST00000422582.5:c.716G>A | ENSP00000406676.1:p.Arg239Gln | |
| ENST00000429084.5:c.1121G>A | ENSP00000403663.1:p.Arg374Gln | |
| ENST00000438383.5:c.896G>A | ENSP00000401613.1:p.Arg299Gln | |
| ENST00000445208.5:c.*709G>A | ENSP00000400598.1:n.*709G>A | |
| ENST00000445295.1:c.277G>A | ||
| ENST00000450807.5:c.356G>A | ENSP00000391585.1:p.Arg119Gln | |
| ENST00000489387.1:n.390G>A | ||
| NM_004722.3:c.1100G>A | NP_004713.2:p.Arg367Gln | |
| XM_005250689.3:c.1121G>A | XP_005250746.1:p.Arg374Gln | |
| XM_005250690.3:c.896G>A | XP_005250747.1:p.Arg299Gln | |
| XM_006716175.2:c.1121G>A | XP_006716238.1:p.Arg374Gln | |
| XM_011516685.1:c.1121G>A | XP_011514987.1:p.Arg374Gln | |
| XM_011516686.1:c.716G>A | XP_011514988.1:p.Arg239Gln | |
| XM_011516687.1:c.425G>A | XP_011514989.1:p.Arg142Gln | |
| NM_001363671.1:c.1121G>A | NP_001350600.1:p.Arg374Gln | |
| XM_005250689.4:c.1121G>A | XP_005250746.1:p.Arg374Gln | |
| XM_005250690.4:c.896G>A | XP_005250747.1:p.Arg299Gln | |
| XM_006716175.4:c.1121G>A | XP_006716238.1:p.Arg374Gln | |
| XM_017012790.2:c.716G>A | XP_016868279.1:p.Arg239Gln | |
| XM_017012791.2:c.425G>A | XP_016868280.1:p.Arg142Gln | |
| XM_024446995.1:c.1100G>A | XP_024302763.1:p.Arg367Gln | |
| XM_024446996.1:c.425G>A | XP_024302764.1:p.Arg142Gln | |
| NM_004722.4:c.1100G>A MANE Select | NP_004713.2:p.Arg367Gln | |
| NM_001363671.2:c.1121G>A | NP_001350600.1:p.Arg374Gln |