Canonical Allele Identifier:
CA1305906800
Gene:
Linked Data
dbSNP Id:
rs1420441096
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.168260568A>T , CM000664.2:g.168260568A>T | GRCh38 |
| NC_000002.11:g.169117078A>T , CM000664.1:g.169117078A>T | GRCh37 |
| NC_000002.10:g.168825324A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001739763.1:n.912-4528A>T | ||
| XR_001739764.1:n.318-4528A>T | ||
| XR_001739765.1:n.436-4528A>T |