Linked Data
ClinVar Variation Id:
46383
dbSNP Id:
rs376318779
ExAC:
5:89992918 A / T
gnomAD v2:
5-89992918-A-T
gnomAD v3:
5-90697101-A-T
gnomAD v4:
5-90697101-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.90697101A>T , CM000667.2:g.90697101A>T | GRCh38 |
| NC_000005.9:g.89992918A>T , CM000667.1:g.89992918A>T | GRCh37 |
| NC_000005.8:g.90028674A>T | NCBI36 |
| NG_007083.1:g.143302A>T | |
| NG_007083.2:g.172758A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405460.9:c.8110A>T MANE Select | ENSP00000384582.2:p.Ile2704Phe | |
| ENST00000639431.1:c.265+20892A>T | ENSP00000491057.1:n.265+20892A>T | |
| ENST00000639473.1:n.3569A>T | ||
| ENST00000640012.1:c.1917A>T | ||
| ENST00000640374.1:n.1254A>T | ||
| ENST00000640403.1:c.5401A>T | ENSP00000492531.1:p.Ile1801Phe | |
| ENST00000640779.1:c.2839A>T | ||
| ENST00000405460.6:c.8110A>T | ENSP00000384582.2:p.Ile2704Phe | |
| ENST00000509621.1:c.807A>T | ||
| NM_032119.3:c.8110A>T | NP_115495.3:p.Ile2704Phe | |
| NR_003149.1:n.8123A>T | ||
| XM_011543675.1:c.8107A>T | XP_011541977.1:p.Ile2703Phe | |
| XM_011543676.1:c.8029A>T | XP_011541978.1:p.Ile2677Phe | |
| XM_011543677.1:c.5413A>T | XP_011541979.1:p.Ile1805Phe | |
| XM_011543678.1:c.8110A>T | XP_011541980.1:p.Ile2704Phe | |
| XM_011543679.1:c.8110A>T | XP_011541981.1:p.Ile2704Phe | |
| NM_032119.4:c.8110A>T MANE Select | NP_115495.3:p.Ile2704Phe | |
| XM_017009963.2:c.8110A>T | XP_016865452.1:p.Ile2704Phe | |
| XM_017009964.2:c.8107A>T | XP_016865453.1:p.Ile2703Phe | |
| XM_017009965.1:c.8107A>T | XP_016865454.1:p.Ile2703Phe | |
| XM_017009966.2:c.8029A>T | XP_016865455.1:p.Ile2677Phe | |
| XM_017009967.1:c.8014A>T | XP_016865456.1:p.Ile2672Phe | |
| XM_017009968.2:c.8110A>T | XP_016865457.1:p.Ile2704Phe | |
| XM_017009969.2:c.8110A>T | XP_016865458.1:p.Ile2704Phe | |
| XM_017009970.2:c.8110A>T | XP_016865459.1:p.Ile2704Phe | |
| XM_017009971.2:c.8110A>T | XP_016865460.1:p.Ile2704Phe | |
| XM_017009972.1:c.1228A>T | XP_016865461.1:p.Ile410Phe | |
| XM_017009973.1:c.1228A>T | XP_016865462.1:p.Ile410Phe | |
| XM_017009974.2:c.8110A>T | XP_016865463.1:p.Ile2704Phe | |
| NR_003149.2:n.8126A>T |