Canonical Allele Identifier:
CA1462694223
Gene:
Linked Data
dbSNP Id:
rs1577990962
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.62558120A>T , CM000666.2:g.62558120A>T | GRCh38 |
| NC_000004.11:g.63423838A>T , CM000666.1:g.63423838A>T | GRCh37 |
| NC_000004.10:g.63106433A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938814.1:n.161-5724A>T |