Canonical Allele Identifier:
CA707405550
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60631965T>A , CM000676.2:g.60631965T>A | GRCh38 |
| NC_000014.8:g.61098683T>A , CM000676.1:g.61098683T>A | GRCh37 |
| NC_000014.7:g.60168436T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537451.1:c.1201+9598A>T | XP_011535753.1:n.1201+9598A>T | |
| XM_011537451.3:c.1201+9598A>T | XP_011535753.1:n.1201+9598A>T |