Canonical Allele Identifier:
CA1557963333
Gene:
Linked Data
dbSNP Id:
rs1158541783
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.79549827G>T , CM000667.2:g.79549827G>T | GRCh38 |
| NC_000005.9:g.78845650G>T , CM000667.1:g.78845650G>T | GRCh37 |
| NC_000005.8:g.78881406G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948497.1:n.72+2183G>T | ||
| XR_948498.1:n.159+1990G>T | ||
| XR_948499.1:n.67+1525G>T | ||
| XR_948497.2:n.72+2183G>T | ||
| XR_948498.2:n.159+1990G>T | ||
| XR_948499.2:n.225+1525G>T |