Canonical Allele Identifier:
CA1205766075
Gene:
Linked Data
dbSNP Id:
rs1648348136
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168649567A>T , CM000663.2:g.168649567A>T | GRCh38 |
| NC_000001.10:g.168618805A>T , CM000663.1:g.168618805A>T | GRCh37 |
| NC_000001.9:g.166885429A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922259.1:n.201-8292T>A | ||
| XR_922259.2:n.332-8292T>A |