Linked Data
ClinVar Variation Id:
6328
dbSNP Id:
rs121908640
gnomAD v2:
9-133370370-C-T
gnomAD v3:
9-130494983-C-T
gnomAD v4:
9-130494983-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130494983C>T , CM000671.2:g.130494983C>T | GRCh38 |
| NC_000009.11:g.133370370C>T , CM000671.1:g.133370370C>T | GRCh37 |
| NC_000009.10:g.132360191C>T | NCBI36 |
| NG_011542.1:g.55277C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352480.10:c.1087C>T MANE Select | ENSP00000253004.6:p.Arg363Trp | |
| ENST00000352480.9:c.1087C>T | ENSP00000253004.6:p.Arg363Trp | |
| ENST00000372386.6:n.358C>T | ||
| ENST00000372393.7:c.1087C>T | ENSP00000361469.2:p.Arg363Trp | |
| ENST00000372394.5:c.1087C>T | ENSP00000361471.1:p.Arg363Trp | |
| NM_000050.4:c.1087C>T | NP_000041.2:p.Arg363Trp | |
| NM_054012.3:c.1087C>T | NP_446464.1:p.Arg363Trp | |
| XM_005272200.2:c.1087C>T | XP_005272257.1:p.Arg363Trp | |
| XM_011518705.1:c.1201C>T | XP_011517007.1:p.Arg401Trp | |
| XR_930393.1:n.1060-2726G>A | ||
| XM_005272200.3:c.1087C>T | XP_005272257.1:p.Arg363Trp | |
| XM_011518705.2:c.1201C>T | XP_011517007.1:p.Arg401Trp | |
| XM_017014729.1:c.1183C>T | XP_016870218.1:p.Arg395Trp | |
| XR_930393.2:n.1102-2726G>A | ||
| NM_054012.4:c.1087C>T MANE Select | NP_446464.1:p.Arg363Trp |