Canonical Allele Identifier:
CA1218511439
Gene:
Linked Data
dbSNP Id:
rs1658966684
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.198499945A>G , CM000663.2:g.198499945A>G | GRCh38 |
| NC_000001.10:g.198469075A>G , CM000663.1:g.198469075A>G | GRCh37 |
| NC_000001.9:g.196735698A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922398.1:n.679+19606T>C | ||
| XR_922398.2:n.341+19606T>C |