Canonical Allele Identifier:
CA1264999445
Gene:
Linked Data
dbSNP Id:
rs12052359
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.81645798C>T , CM000664.2:g.81645798C>T | GRCh38 |
| NC_000002.11:g.81872922C>T , CM000664.1:g.81872922C>T | GRCh37 |
| NC_000002.10:g.81726433C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_940294.1:n.563+66189C>T | ||
| XR_940295.1:n.485+97051C>T | ||
| XR_001739571.1:n.485+97051C>T |