Canonical Allele Identifier:
CA2697393040
Gene:
Linked Data
dbSNP Id:
rs2101874752
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168649267G>A , CM000663.2:g.168649267G>A | GRCh38 |
| NC_000001.10:g.168618505G>A , CM000663.1:g.168618505G>A | GRCh37 |
| NC_000001.9:g.166885129G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922259.1:n.201-7992C>T | ||
| XR_922259.2:n.332-7992C>T |