Linked Data
ClinVar Variation Id:
16793
dbSNP Id:
rs41556519
ExAC:
19:45855610 G / A
gnomAD v2:
19-45855610-G-A
gnomAD v3:
19-45352352-G-A
gnomAD v4:
19-45352352-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45352352G>A , CM000681.2:g.45352352G>A | GRCh38 |
| NC_000019.9:g.45855610G>A , CM000681.1:g.45855610G>A | GRCh37 |
| NC_000019.8:g.50547450G>A | NCBI36 |
| NG_007067.2:g.23236C>T , LRG_461:g.23236C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000391944.8:c.2047C>T | ENSP00000375808.4:p.Arg683Trp | |
| ENST00000682414.1:c.2047C>T | ENSP00000507019.1:p.Arg683Trp | |
| ENST00000682508.1:n.2076C>T | ||
| ENST00000684218.1:c.*1305C>T | ENSP00000507804.1:n.*1305C>T | |
| ENST00000684264.1:n.1603C>T | ||
| ENST00000684407.1:c.1924C>T | ENSP00000507775.1:p.Arg642Trp | |
| ENST00000684458.1:c.*533C>T | ENSP00000508260.1:n.*533C>T | |
| ENST00000684468.1:n.1759C>T | ||
| ENST00000391945.10:c.2047C>T MANE Select | ENSP00000375809.4:p.Arg683Trp | |
| ENST00000646507.1:n.2144C>T | ||
| ENST00000391941.6:c.1975C>T | ENSP00000375805.2:p.Arg659Trp | |
| ENST00000391942.6:n.1218C>T | ||
| ENST00000391944.7:c.1813C>T | ENSP00000375808.3:p.Arg605Trp | |
| ENST00000391945.8:c.2047C>T | ENSP00000375809.3:p.Arg683Trp | |
| ENST00000588652.5:n.2135C>T | ||
| NM_000400.3:c.2047C>T , LRG_461t1:c.2047C>T | NP_000391.1:p.Arg683Trp | |
| XM_011526611.1:c.1969C>T | XP_011524913.1:p.Arg657Trp | |
| XM_011526611.2:c.1969C>T | XP_011524913.1:p.Arg657Trp | |
| XM_017026467.1:c.1924C>T | XP_016881956.1:p.Arg642Trp | |
| XR_001753633.2:n.2094C>T | ||
| XR_001753634.2:n.2030C>T | ||
| NM_000400.4:c.2047C>T MANE Select | NP_000391.1:p.Arg683Trp |