Canonical Allele Identifier:
CA1841175632
Gene:
Linked Data
dbSNP Id:
rs1819678289
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551512C>T , CM000671.2:g.25551512C>T | GRCh38 |
| NC_000009.11:g.25551510C>T , CM000671.1:g.25551510C>T | GRCh37 |
| NC_000009.10:g.25541510C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929525.1:n.50-940G>A | ||
| XR_929525.2:n.674-940G>A |