Canonical Allele Identifier:
CA1595159121
Gene:
Linked Data
dbSNP Id:
rs1757451195
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159580773T>G , CM000667.2:g.159580773T>G | GRCh38 |
| NC_000005.9:g.159007781T>G , CM000667.1:g.159007781T>G | GRCh37 |
| NC_000005.8:g.158940359T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_941139.1:n.2075+338T>G | ||
| XR_941140.1:n.2075+338T>G | ||
| XR_941141.1:n.570+338T>G | ||
| XR_941139.2:n.2229+338T>G |