Canonical Allele Identifier:
CA1427629890
Gene:
Linked Data
dbSNP Id:
rs1715477691
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.187931553T>A , CM000665.2:g.187931553T>A | GRCh38 |
| NC_000003.11:g.187649341T>A , CM000665.1:g.187649341T>A | GRCh37 |
| NC_000003.10:g.189132035T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_924814.1:n.1361A>T |