Canonical Allele Identifier:
CA1205766048
Gene:
Linked Data
dbSNP Id:
rs949672798
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168649479A>C , CM000663.2:g.168649479A>C | GRCh38 |
| NC_000001.10:g.168618717A>C , CM000663.1:g.168618717A>C | GRCh37 |
| NC_000001.9:g.166885341A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922259.1:n.201-8204T>G | ||
| XR_922259.2:n.332-8204T>G |