Canonical Allele Identifier:
CA1841175423
Gene:
Linked Data
dbSNP Id:
rs1278759011
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551141T>A , CM000671.2:g.25551141T>A | GRCh38 |
| NC_000009.11:g.25551139T>A , CM000671.1:g.25551139T>A | GRCh37 |
| NC_000009.10:g.25541139T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929525.1:n.50-569A>T | ||
| XR_929525.2:n.674-569A>T |