Canonical Allele Identifier: CA122000
Gene:

Linked Data

ClinVar Variation Id: 12247
ClinVar RCV Id: RCV000013034
dbSNP Id: rs16260

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737131C>A , CM000678.2:g.68737131C>A GRCh38
NC_000016.9:g.68771034C>A , CM000678.1:g.68771034C>A GRCh37
NC_000016.8:g.67328535C>A NCBI36
NG_008021.1:g.4840C>A , LRG_301:g.4840C>A