Linked Data
ClinVar Variation Id:
2754103
ClinVar RCV Id:
RCV003569168
dbSNP Id:
rs372458386
ExAC:
19:36592646 C / T
gnomAD v2:
19-36592646-C-T
gnomAD v3:
19-36101744-C-T
gnomAD v4:
19-36101744-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.36101744C>T , CM000681.2:g.36101744C>T | GRCh38 |
| NC_000019.9:g.36592646C>T , CM000681.1:g.36592646C>T | GRCh37 |
| NC_000019.8:g.41284486C>T | NCBI36 |
| NG_028101.1:g.51864C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270301.12:c.3052C>T | ENSP00000270301.6:p.Arg1018Trp | |
| ENST00000401500.7:c.3052C>T MANE Select | ENSP00000384792.1:p.Arg1018Trp | |
| ENST00000587391.6:c.*2088C>T | ENSP00000465525.1:n.*2088C>T | |
| ENST00000679357.1:c.842C>T | ||
| ENST00000679422.1:c.762-270C>T | ||
| ENST00000679682.1:c.3037C>T | ENSP00000506226.1:p.Arg1013Trp | |
| ENST00000679714.1:c.3046C>T | ENSP00000506627.1:p.Arg1016Trp | |
| ENST00000679757.1:c.2701C>T | ENSP00000505158.1:p.Arg901Trp | |
| ENST00000679858.1:c.*2195C>T | ENSP00000505655.1:n.*2195C>T | |
| ENST00000680211.1:c.-348C>T | ENSP00000506102.1:n.-348C>T | |
| ENST00000680349.1:n.1035C>T | ||
| ENST00000680403.1:c.3052C>T | ENSP00000505677.1:p.Arg1018Trp | |
| ENST00000680564.1:c.2971+427C>T | ENSP00000505582.1:n.2971+427C>T | |
| ENST00000680590.1:c.*1447C>T | ENSP00000505350.1:n.*1447C>T | |
| ENST00000680773.1:n.729C>T | ||
| ENST00000680806.1:c.*1801-270C>T | ENSP00000506418.1:n.*1801-270C>T | |
| ENST00000680997.1:n.399C>T | ||
| ENST00000681088.1:c.714C>T | ||
| ENST00000681625.1:c.*384C>T | ENSP00000505555.1:n.*384C>T | |
| ENST00000270301.11:c.3052C>T | ENSP00000270301.6:p.Arg1018Trp | |
| ENST00000401500.6:c.3052C>T | ENSP00000384792.1:p.Arg1018Trp | |
| ENST00000587391.5:c.*2088C>T | ENSP00000465525.1:n.*2088C>T | |
| NM_001083961.1:c.3052C>T | NP_001077430.1:p.Arg1018Trp | |
| NM_173636.4:c.3052C>T | NP_775907.4:p.Arg1018Trp | |
| XM_005258809.2:c.2972-270C>T | XP_005258866.1:n.2972-270C>T | |
| XM_011526837.1:c.3037C>T | XP_011525139.1:p.Arg1013Trp | |
| XM_011526838.1:c.2971+427C>T | XP_011525140.1:n.2971+427C>T | |
| XM_011526839.1:c.2701C>T | XP_011525141.1:p.Arg901Trp | |
| XM_011526840.1:c.2044C>T | XP_011525142.1:p.Arg682Trp | |
| XM_011526841.1:c.1630C>T | XP_011525143.1:p.Arg544Trp | |
| XM_011526842.1:c.1483C>T | XP_011525144.1:p.Arg495Trp | |
| XM_011526843.1:c.799C>T | XP_011525145.1:p.Arg267Trp | |
| XM_011526844.1:c.799C>T | XP_011525146.1:p.Arg267Trp | |
| XM_011526840.2:c.2044C>T | XP_011525142.1:p.Arg682Trp | |
| XM_011526841.2:c.1630C>T | XP_011525143.1:p.Arg544Trp | |
| XM_011526844.2:c.799C>T | XP_011525146.1:p.Arg267Trp | |
| XM_017026665.1:c.3052C>T | XP_016882154.1:p.Arg1018Trp | |
| NM_001083961.2:c.3052C>T MANE Select | NP_001077430.1:p.Arg1018Trp | |
| NM_173636.5:c.3052C>T | NP_775907.4:p.Arg1018Trp |