Canonical Allele Identifier:
CA1841175543
Gene:
Linked Data
dbSNP Id:
rs185620911
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551371G>T , CM000671.2:g.25551371G>T | GRCh38 |
| NC_000009.11:g.25551369G>T , CM000671.1:g.25551369G>T | GRCh37 |
| NC_000009.10:g.25541369G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_929525.1:n.50-799C>A | ||
| XR_929525.2:n.674-799C>A |