Canonical Allele Identifier:
CA1205766001
Gene:
Linked Data
dbSNP Id:
rs1648344821
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168649402T>G , CM000663.2:g.168649402T>G | GRCh38 |
| NC_000001.10:g.168618640T>G , CM000663.1:g.168618640T>G | GRCh37 |
| NC_000001.9:g.166885264T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922259.1:n.201-8127A>C | ||
| XR_922259.2:n.332-8127A>C |