Canonical Allele Identifier:
CA2721793276
Gene:
Linked Data
dbSNP Id:
rs2132201038
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.57812997A>T , CM000672.2:g.57812997A>T | GRCh38 |
| NC_000010.10:g.59572757A>T , CM000672.1:g.59572757A>T | GRCh37 |
| NC_000010.9:g.59242763A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945979.1:n.68+34295T>A | ||
| XR_001747454.1:n.85+34295T>A |