Linked Data
ClinVar Variation Id:
285514
dbSNP Id:
rs199798095
ExAC:
5:89910784 G / A
gnomAD v2:
5-89910784-G-A
gnomAD v3:
5-90614967-G-A
gnomAD v4:
5-90614967-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.90614967G>A , CM000667.2:g.90614967G>A | GRCh38 |
| NC_000005.9:g.89910784G>A , CM000667.1:g.89910784G>A | GRCh37 |
| NC_000005.8:g.89946540G>A | NCBI36 |
| NG_007083.1:g.61168G>A | |
| NG_007083.2:g.90624G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405460.9:c.155G>A MANE Select | ENSP00000384582.2:p.Arg52His | |
| ENST00000638316.1:n.365G>A | ||
| ENST00000640109.1:n.251G>A | ||
| ENST00000640281.1:n.214G>A | ||
| ENST00000405460.6:c.155G>A | ENSP00000384582.2:p.Arg52His | |
| ENST00000508842.5:c.167G>A | ENSP00000425936.1:p.Arg56His | |
| NM_032119.3:c.155G>A | NP_115495.3:p.Arg52His | |
| NR_003149.1:n.251G>A | ||
| XM_011543675.1:c.155G>A | XP_011541977.1:p.Arg52His | |
| XM_011543676.1:c.155G>A | XP_011541978.1:p.Arg52His | |
| XM_011543678.1:c.155G>A | XP_011541980.1:p.Arg52His | |
| XM_011543679.1:c.155G>A | XP_011541981.1:p.Arg52His | |
| NM_032119.4:c.155G>A MANE Select | NP_115495.3:p.Arg52His | |
| XM_017009963.2:c.155G>A | XP_016865452.1:p.Arg52His | |
| XM_017009964.2:c.155G>A | XP_016865453.1:p.Arg52His | |
| XM_017009965.1:c.152G>A | XP_016865454.1:p.Arg51His | |
| XM_017009966.2:c.155G>A | XP_016865455.1:p.Arg52His | |
| XM_017009967.1:c.155G>A | XP_016865456.1:p.Arg52His | |
| XM_017009968.2:c.155G>A | XP_016865457.1:p.Arg52His | |
| XM_017009969.2:c.155G>A | XP_016865458.1:p.Arg52His | |
| XM_017009970.2:c.155G>A | XP_016865459.1:p.Arg52His | |
| XM_017009971.2:c.155G>A | XP_016865460.1:p.Arg52His | |
| XM_017009974.2:c.155G>A | XP_016865463.1:p.Arg52His | |
| NR_003149.2:n.254G>A |