Canonical Allele Identifier:
CA1691656444
Gene:
Linked Data
dbSNP Id:
rs1803285696
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17957849C>A , CM000669.2:g.17957849C>A | GRCh38 |
| NC_000007.13:g.17997472C>A , CM000669.1:g.17997472C>A | GRCh37 |
| NC_000007.12:g.17963997C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927078.1:n.271-821C>A |