Canonical Allele Identifier:
CA1751418917
Gene:
Linked Data
dbSNP Id:
rs1801684930
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.148807152G>A , CM000669.2:g.148807152G>A | GRCh38 |
| NC_000007.13:g.148504244G>A , CM000669.1:g.148504244G>A | GRCh37 |
| NC_000007.12:g.148135177G>A | NCBI36 |
| NG_032043.1:g.82198C>T , LRG_531:g.82198C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928101.1:n.515+2067G>A | ||
| XR_928102.1:n.722+2067G>A |