Canonical Allele Identifier:
CA1931617875
Gene:
Linked Data
dbSNP Id:
rs2041646277
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100101711C>T , CM000672.2:g.100101711C>T | GRCh38 |
| NC_000010.10:g.101861468C>T , CM000672.1:g.101861468C>T | GRCh37 |
| NC_000010.9:g.101851458C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_946245.1:n.185+5474C>T |