Canonical Allele Identifier:
CA2718853000
Gene:
Linked Data
dbSNP Id:
rs1168849656
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551289T>G , CM000671.2:g.25551289T>G | GRCh38 |
| NC_000009.11:g.25551287T>G , CM000671.1:g.25551287T>G | GRCh37 |
| NC_000009.10:g.25541287T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_929525.1:n.50-717A>C | ||
| XR_929525.2:n.674-717A>C |