Canonical Allele Identifier:
CA257451169
Gene:
Linked Data
dbSNP Id:
rs920494065
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.20793435T>A , CM000676.2:g.20793435T>A | GRCh38 |
| NC_000014.8:g.21261594T>A , CM000676.1:g.21261594T>A | GRCh37 |
| NC_000014.7:g.20331434T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943584.1:n.585+649T>A | ||
| XR_943585.1:n.585+649T>A | ||
| XR_001750620.1:n.3271+649T>A | ||
| XR_001750621.1:n.3271+649T>A | ||
| XR_001750622.1:n.637+6469A>T | ||
| XR_001750623.1:n.637+6469A>T | ||
| XR_001750624.1:n.637+6469A>T |