Canonical Allele Identifier:
CA117764802
Gene:
Linked Data
dbSNP Id:
rs172881
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.41107378C>T , CM000667.2:g.41107378C>T | GRCh38 |
| NC_000005.9:g.41107480C>T , CM000667.1:g.41107480C>T | GRCh37 |
| NC_000005.8:g.41143237C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_925944.1:n.618-5250C>T | ||
| XR_925945.1:n.125-5250C>T | ||
| XR_925946.1:n.576-5250C>T | ||
| XR_925948.1:n.618-5250C>T | ||
| XR_001742650.1:n.618-5250C>T | ||
| XR_001742651.1:n.131-5250C>T |