Linked Data
ClinVar Variation Id:
580556
ClinVar RCV Id:
RCV000704133
dbSNP Id:
rs750026880
ExAC:
11:68675678 C / T
gnomAD v2:
11-68675678-C-T
gnomAD v3:
11-68908210-C-T
gnomAD v4:
11-68908210-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68908210C>T , CM000673.2:g.68908210C>T | GRCh38 |
| NC_000011.9:g.68675678C>T , CM000673.1:g.68675678C>T | GRCh37 |
| NC_000011.8:g.68432254C>T | NCBI36 |
| NG_007976.1:g.9360C>T , LRG_250:g.9360C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.322C>T MANE Select | ENSP00000255078.4:p.Arg108Trp | |
| ENST00000539224.2:c.285C>T | ||
| ENST00000674583.1:c.285C>T | ||
| ENST00000674597.1:c.133C>T | ||
| ENST00000674955.1:c.322C>T | ENSP00000502463.1:p.Arg108Trp | |
| ENST00000675142.1:n.285C>T | ||
| ENST00000675469.1:c.198C>T | ||
| ENST00000675615.1:c.322C>T | ENSP00000502413.1:p.Arg108Trp | |
| ENST00000675674.1:n.285C>T | ||
| ENST00000675873.1:c.285C>T | ||
| ENST00000676173.1:n.366C>T | ||
| ENST00000676228.1:c.322C>T | ENSP00000502375.1:p.Arg108Trp | |
| ENST00000255078.7:c.322C>T | ENSP00000255078.3:p.Arg108Trp | |
| ENST00000539224.1:c.322C>T | ENSP00000440465.1:p.Arg108Trp | |
| ENST00000544541.1:c.*62C>T | ENSP00000443343.1:n.*62C>T | |
| NM_002180.2:c.322C>T , LRG_250t1:c.322C>T | NP_002171.2:p.Arg108Trp | |
| XM_005273974.2:c.-690C>T | XP_005274031.1:n.-690C>T | |
| XM_005273976.1:c.322C>T | XP_005274033.1:p.Arg108Trp | |
| XR_247198.1:n.424C>T | ||
| XR_949903.1:n.424C>T | ||
| XM_005273976.2:c.322C>T | XP_005274033.1:p.Arg108Trp | |
| XM_017017669.2:c.-592C>T | XP_016873158.1:n.-592C>T | |
| XM_017017671.2:c.322C>T | XP_016873160.1:p.Arg108Trp | |
| XR_949903.3:n.420C>T | ||
| NM_002180.3:c.322C>T MANE Select | NP_002171.2:p.Arg108Trp |