Canonical Allele Identifier:
CA2136398881
Gene:
Linked Data
dbSNP Id:
rs1566901449
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50856925C>T , CM000676.2:g.50856925C>T | GRCh38 |
| NC_000014.8:g.51323643C>T , CM000676.1:g.51323643C>T | GRCh37 |
| NC_000014.7:g.50393393C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_943848.1:n.282+1173G>A | ||
| XR_943848.2:n.643+1173G>A |