Canonical Allele Identifier:
CA2140863498
Gene:
Linked Data
dbSNP Id:
rs10483727
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60606157T>A , CM000676.2:g.60606157T>A | GRCh38 |
| NC_000014.8:g.61072875T>A , CM000676.1:g.61072875T>A | GRCh37 |
| NC_000014.7:g.60142628T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011537451.1:c.1202-30865A>T | XP_011535753.1:n.1202-30865A>T | |
| XM_011537451.3:c.1202-30865A>T | XP_011535753.1:n.1202-30865A>T |