Canonical Allele Identifier:
CA1462694258
Gene:
Linked Data
dbSNP Id:
rs1577990998
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.62558183G>T , CM000666.2:g.62558183G>T | GRCh38 |
| NC_000004.11:g.63423901G>T , CM000666.1:g.63423901G>T | GRCh37 |
| NC_000004.10:g.63106496G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938814.1:n.161-5661G>T |