Linked Data
ClinVar Variation Id:
206327
dbSNP Id:
rs796052812
gnomAD v3:
X-100407484-G-A
gnomAD v4:
X-100407484-G-A
COSMIC:
COSM3144022
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.100407484G>A , CM000685.2:g.100407484G>A | GRCh38 |
| NC_000023.10:g.99662482G>A , CM000685.1:g.99662482G>A | GRCh37 |
| NC_000023.9:g.99549138G>A | NCBI36 |
| NG_021319.1:g.7790C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000255531.8:c.1114C>T | ENSP00000255531.7:p.Arg372Trp | |
| ENST00000373034.8:c.1114C>T MANE Select | ENSP00000362125.4:p.Arg372Trp | |
| ENST00000420881.6:c.1114C>T | ENSP00000400327.2:p.Arg372Trp | |
| NM_001105243.1:c.1114C>T | NP_001098713.1:p.Arg372Trp | |
| NM_001184880.1:c.1114C>T | NP_001171809.1:p.Arg372Trp | |
| NM_020766.2:c.1114C>T | NP_065817.2:p.Arg372Trp | |
| XM_011530997.1:c.1114C>T | XP_011529299.1:p.Arg372Trp | |
| XM_011530997.2:c.1114C>T | XP_011529299.1:p.Arg372Trp | |
| NM_001105243.2:c.1114C>T | NP_001098713.1:p.Arg372Trp | |
| NM_001184880.2:c.1114C>T MANE Select | NP_001171809.1:p.Arg372Trp | |
| NM_020766.3:c.1114C>T | NP_065817.2:p.Arg372Trp |