Canonical Allele Identifier:
CA2711012226
Gene:
Linked Data
dbSNP Id:
rs2127453797
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.465899C>T , CM000668.2:g.465899C>T | GRCh38 |
| NC_000006.11:g.465899C>T , CM000668.1:g.465899C>T | GRCh37 |
| NC_000006.10:g.410899C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926364.1:n.2714+12174C>T | ||
| XR_926365.1:n.2548+12174C>T | ||
| XR_001743914.1:n.482-9309C>T |