Linked Data
ClinVar Variation Id:
1095532
ClinVar RCV Id:
RCV001416435
dbSNP Id:
rs537863698
gnomAD v4:
1-216199637-C-A
COSMIC:
COSM383764
MyVariant Identifiers:
chr1:g.216372979C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216199637C>A , CM000663.2:g.216199637C>A | GRCh38 |
| NC_000001.10:g.216372979C>A , CM000663.1:g.216372979C>A | GRCh37 |
| NC_000001.9:g.214439602C>A | NCBI36 |
| NG_009497.1:g.228760G>T | |
| NG_009497.2:g.228812G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.3801G>T (USH2A) MANE Select | ENSP00000305941.3:p.Ala1267= | |
| ENST00000674083.1:c.3801G>T (USH2A) | ENSP00000501296.1:p.Ala1267= | |
| ENST00000307340.7:c.3801G>T (USH2A) | ENSP00000305941.3:p.Ala1267= | |
| ENST00000366942.3:c.3801G>T (USH2A) | ENSP00000355909.3:p.Ala1267= | |
| NM_007123.5:c.3801G>T (USH2A) | NP_009054.5:p.Ala1267= | |
| NM_206933.2:c.3801G>T (USH2A) | NP_996816.2:p.Ala1267= | |
| XR_922595.1:n.354+3712C>A (USH2A-AS1) | ||
| XR_922596.1:n.354+3712C>A (USH2A-AS1) | ||
| XR_922597.1:n.354+3712C>A (USH2A-AS1) | ||
| XR_922598.1:n.484+3712C>A (USH2A-AS1) | ||
| XR_922595.3:n.1076+3712C>A (USH2A-AS1) | ||
| XR_922596.3:n.1076+3712C>A (USH2A-AS1) | ||
| NM_206933.3:c.3801G>T (USH2A) | NP_996816.2:p.Ala1267= | |
| NM_007123.6:c.3801G>T (USH2A) | NP_009054.6:p.Ala1267= | |
| NM_206933.4:c.3801G>T (USH2A) MANE Select | NP_996816.3:p.Ala1267= |